analisa dib update

12.   Px ugd mawar tanpa ptm

Dalam kasus ini dokter telah melanggar kode etik kedokteran pasal 7c yaitu seorang dokter harus menghormati hak pasien untuk sembuh dan pasal 13 yaitu dokter wajib beri pertolongan darurat, padahal IC bagi pasien kondisi gawat darurat tidak diperlukan (etik)

Pelanggaran pasal 359 KUHP yaitu menyebabkan kematian seseorang karena kelalaiannya ancaman hukuman pidana penjara 5 tahun/kurungan paling lama 1 tahun.

Pelanggaran pasal 1366 KUH perdata, pasal 1370 KUH perdata, sesuai pasal 1367 KUH perdata pihak rumah sakit juga menanggung ganti rugi pada korban karena dokter tsb kerja di rs tsb

13.   Aborsi

Seorang bidan dalam kasus ini telah melanggar kode etik bidan terhadap profesinya dan kode etik bidan terhadap bangsa, pemerintah dan tanah air karna tidak menjaga nama baik dan

menjunjung citra profesinya, bidan tersebut melakukan aborsi dan membunuh janin yang akan menjadi generasi bangsa selanjutnya.

Pelanggaran pasal pasal 229 ayat 1, 2, dan 3, pasal 347, pasal 348, pasal 349 karena bidan tersebut telah melakukan aborsi ilegal (membantu melakukan kejahatan),  Dengan sengaja telah merampas nyawa seorang anak. Sedang si ibu telah melanggar pasal 341 dan pasal 346 karena telah menghendaki aborsi yg tidak sesuai ketentuan (pidana)

        Pasal 1366 yaitu kerugian seseorang akibat kelalaiannya 

Pembedahan benjolan

Sanksi Pidana

Seorang tenaga kesehatan yang menorehkan benda tajam, membius pasien tanpa persetujuan dapat disamakan melakukan penganiayaan yang dapat dijerat pasal 351 KUHP

Sangsi Perdata

Pasal 1371 Kitab Undang-Undang Hukum Perdata

Sangsi Administratif

Pasal 13 Permenkes tentang pendidikan mengatur tentang sangsi administrasi : terhadap dokter yang melakukan tindakan medik tanpa persetujuan pasien ataukeluarganya dapat dikenakan sangsi administratip, berupa pencabutan ijin praktek.

mik dib reupload

1.       Agama : Adalah suatu norma yang berdasarkan ajaran aqidah suatu agama,mutlak, mengharuskan penganut taat

Kesusilaan : Norma ini didasarkan pada hati nurani atau ahlak manusia.

Kesopanan : Adalah norma yang berpangkal dari aturan tingkah laku yang berlaku di masyrakat

Hukum : himpunan petunjuk hidup atau perintah dan larangan yang mengatur tata tertib dalam suatu masyarakat (negara)bersifat memaksa dan mengikat

2.       0 : no UKRM u/ kelola RM

1 : ukrm berfungsi  rangkap dg kegiatan lain

2 : ada UKRM fungsi terbatas

3 : ada BPPRM terbaru, tidak lgkap

4 : ada UKRM berfungsi hampir memadai

5 : UKRM berfungsi optimal

Umum : meningkatkan pelayanan RS

Khusus : beri jaminan kepuasan pd masy., beri pengakuan thd rs yg terapkan standar pelayanan rs, ciptakan lingkungan RS yang kondusif u/ penyembuhan, pengobatan, sesuai standar Struktur

3.       Hospital law : peraturan rumah sakit yang dibuat oleh pemerintah pusat

Hospital by laws : peraturan rumah sakit yang dibuat oleh intern rumah sakit

Dimilikinya pedoman aspek hukum oleh rumah sakit dalam hubungannya dengan pemilik atau yang mewakili, direktur rumah sakit dan staf medis.
Dimilikinya pedoman aspek hukum dalam pembuatan kebijakan teknis operasional rumah sakit.
Dimilikinya pedoman aspek hukum dalam pengaturan staf medis 

4.      Reliability : kehandalan pelayanan yang dijanjikan segera dan memuaskan

Responsivness : daya tanggap, memberi pelayanan dengan tanggap tanpa bedakan SARA

Assurance : jaminan keamanan, kenyamanan, dan keselamatan pasien

      Emphaty : komunikasi yang baik dan pahami kebutuhan pasien

5.     Tempat kerja :  dalam ruang UK (departemen/sie)[lama]; berbasis informasi [baru]

Model RM : data fisik, teraba, tampak [lama]; konsep data > definisi butiran data/item ( data admin& audit)

Tampilan : data dikumpulkan scr agregasi & dipresentasikan [lama]; pencarian scr elektronik, teknik statistik & permoddelan data [baru]

Isi : formulir & desain RM [lama]; tampilan data, alur data, reenginering, aplikasi penunjang [baru]

       Aspek hukum : kerahasiaan & pelepasan informasi [lama]; sekuritas, audit, program pengawasan, penilaian resiko analisis, pencegahan,
       ukuran p’awasan [baru] 

6.       Dalam melakasanakan tugas profesi PMIK selalu bertindak demi kehormatan dan kemuliaan diri dan organisasi, selalu jalankan tugas berdasar ukuran profesi tertinggi, mengutamakan pelayanan daripada meterial selalu beri pelayanan yg sesuai & pelyankes bermutu, selalu menjaga dan dan menyiman BRM serta inf. Yg terkandung didalamnya sesuai perundang2an yg berlaku, junjung tinggi doktrin kerahasiaan dan hak atas informasi yg terkait identitas individu atau sosial, 

Menghayati dan mengamalkan pancasila secara murni dan konsekuen

Menjunjung tinggi nama baik dan kehormatan organisasi 

Memegang teguh AD/ART,peraturan2 dan disiplin organisasi 

Taat melaksanakan tugas dan program organisasi  

Memegang teguh rahasia organisasi

7.    fungsi komite medis

memberi saran pada direktur rumah sakit / kabid yanmed

mengkoordinasikan dan mengarahkan kegiatan yanmed

menangani hal2 yg berkaitan dengan etik kedokteran

susun kebijakan yanmed sebagai standar yg harus dilaksanakan o/ staf medis di rs 

8.   kewajiban tenakes PP RI No.32 tahun 1996 tentang tenaga kesehatan BAB V Pasal 21

  berkewajiban untuk mematuhi standar profesi tenaga kesehatan.  

  menghormati hak pasien

  menjaga kerahasiaan identitas dan data kesehatan pribadi pasien  

  memberikan infomasi yang berkaitan dengan kondisi dan tindakan yang akan dilakukan

  meminta persetujuan terhadap tindakan yang akan dilakukan

  membuat dan memelihara rekam medis 

9.     asas etik kedokteran

          Principle of autonomy : prinsip menghormati keputusan dan pendapat pasien atas apa yang akan dialkukan padanya dengan memberi informasi yang cukup dan pemberian IC

        Principle of veracity : prinsip kejujuran, dokter harus mengatakan sebenarnya mengenai apa yang akan terjadi, apa yang akan dilakukan, serta resiko tindakan tsb. Informasi yang diberikan disesuaikan tingkat pendidikan pasien  

       Principle of justice : dokter harus adil dalam memberi perawatan, tidak membeda2kan pasien

  

10.  Aspek hukum Rekam medis

Permenkes no 269/menkes/PER/III/2008 pengertian rm berkas yg berisi catatan ID, pengobatan  yg diberikan 

Pp no 10 tahun 1966 wajib simpan rahasia kedokteran 

     Uu no 29/2004 praktik kedokteran 
     Pasal 322 KUH pidana Pasal 1367 KUH perdata

Pasal 1365 KUH perdata

Surat keputusan dirjen Yanmed no 78/Yanmed/ RS

Keamanan DRM :

Hanya petugas yg diizinkan masuk ruangan

Dilarang mengutip sebagaian atau seluruh rm kecuali sesuai PERUU

Selama px dirawat kerahasiaan RM di suster perawat

Keputusan menteri kesehatan RI no 034/Birhub/1972

11.  syarat sahnya persetujuan tindakan medis

ada penjelasan dokter terkait resiko dr tindakan

pasien sadar dan tanpa paksaan dari pihak lain

bagi pasien dibawah umur dan tidak sadar dapat diwakili keluarga

ada bukti tertulis yang ditanda tangani 2 belah pihak

12.  hubungan px dengan transaksi terapetik

RS-px : perjanjian perawatan (kamar, tenaga, tindakan) & perjanjian pelayanan medis

Dr-px : hubungan kontrak terapetik inspanning verbitenis jarang resultaat

TKL-PX : perikatan/kontrak yaitu TKL harus berupaya melayani dengan skill dan ilmu yg dimiliki

Dr-p’awat : rujukan/delegasi

 

   

 

 

Congenital malformations, deformations, & chromosomal abnormalities

Q00	Anencephaly and similar malformations
Q00.0	Anencephaly
Q00.1	Craniorachischisis
Q00.2	Iniencephaly
Q01	Encephalocele
Q01.0	Frontal encephalocele
Q01.1	Nasofrontal encephalocele
Q01.2	Occipital encephalocele
Q01.8	Encephalocele of other sites
Q01.9	Encephalocele, unspecified
Q02	Microcephaly
Q03	Congenital hydrocephalus
Q03.0	Malformations of aqueduct of Sylvius
Q03.1	Atresia of foramina of Magendie and Luschka
Q03.8	Other congenital hydrocephalus
Q03.9	Congenital hydrocephalus, unspecified
Q04	Other congenital malformations of brain
Q04.0	Congenital malformations of corpus callosum
Q04.1	Arhinencephaly
Q04.2	Holoprosencephaly
Q04.3	Other reduction deformities of brain
Q04.4	Septo-optic dysplasia
Q04.5	Megalencephaly
Q04.6	Congenital cerebral cysts
Q04.8	Other specified congenital malformations of brain
Q04.9	Congenital malformation of brain, unspecified
Q05	Spina bifida
Q05.0	Cervical spina bifida with hydrocephalus
Q05.1	Thoracic spina bifida with hydrocephalus
Q05.2	Lumbar spina bifida with hydrocephalus
Q05.3	Sacral spina bifida with hydrocephalus
Q05.4	Unspecified spina bifida with hydrocephalus
Q05.5	Cervical spina bifida without hydrocephalus
Q05.6	Thoracic spina bifida without hydrocephalus
Q05.7	Lumbar spina bifida without hydrocephalus
Q05.8	Sacral spina bifida without hydrocephalus
Q05.9	Spina bifida, unspecified
Q06	Other congenital malformations of spinal cord
Q06.0	Amyelia
Q06.1	Hypoplasia and dysplasia of spinal cord
Q06.2	Diastematomyelia
Q06.3	Other congenital cauda equina malformations
Q06.4	Hydromyelia
Q06.8	Other specified congenital malformations of spinal cord
Q06.9	Congenital malformation of spinal cord, unspecified
Q07	Other congenital malformations of nervous system
Q07.0	Arnold-Chiari syndrome
Q07.8	Other specified congenital malformations of nervous system
Q07.9	Congenital malformation of nervous system, unspecified
Q10	Congenital malformations of eyelid, lacrimal apparatus and orbit
Q10.0	Congenital ptosis
Q10.1	Congenital ectropion
Q10.2	Congenital entropion
Q10.3	Other congenital malformations of eyelid
Q10.4	Absence and agenesis of lacrimal apparatus
Q10.5	Congenital stenosis and stricture of lacrimal duct
Q10.6	Other congenital malformations of lacrimal apparatus
Q10.7	Congenital malformation of orbit
Q11	Anophthalmos, microphthalmos and macrophthalmos
Q11.0	Cystic eyeball
Q11.1	Other anophthalmos
Q11.2	Microphthalmos
Q11.3	Macrophthalmos
Q12	Congenital lens malformations
Q12.0	Congenital cataract
Q12.1	Congenital displaced lens
Q12.2	Coloboma of lens
Q12.3	Congenital aphakia
Q12.4	Spherophakia
Q12.8	Other congenital lens malformations
Q12.9	Congenital lens malformation, unspecified
Q13	Congenital malformations of anterior segment of eye
Q13.0	Coloboma of iris
Q13.1	Absence of iris
Q13.2	Other congenital malformations of iris
Q13.3	Congenital corneal opacity
Q13.4	Other congenital corneal malformations
Q13.5	Blue sclera
Q13.8	Other congenital malformations of anterior segment of eye
Q13.9	Congenital malformation of anterior segment of eye, unspecified
Q14	Congenital malformations of posterior segment of eye
Q14.0	Congenital malformation of vitreous humour
Q14.1	Congenital malformation of retina
Q14.2	Congenital malformation of optic disc
Q14.3	Congenital malformation of choroid
Q14.8	Other congenital malformations of posterior segment of eye
Q14.9	Congenital malformation of posterior segment of eye, unspecified
Q15	Other congenital malformations of eye
Q15.0	Congenital glaucoma
Q15.8	Other specified congenital malformations of eye
Q15.9	Congenital malformation of eye, unspecified
Q16	Congenital malformations of ear causing impairment of hearing
Q16.0	Congenital absence of (ear) auricle
Q16.1	Congenital absence, atresia and stricture of auditory canal(external)
Q16.2	Absence of eustachian tube
Q16.3	Congenital malformation of ear ossicles
Q16.4	Other congenital malformations of middle ear
Q16.5	Congenital malformation of inner ear
Q16.9	Congenital malformation of ear causing impairment of hearing,unspecified
Q17	Other congenital malformations of ear
Q17.0	Accessory auricle
Q17.1	Macrotia
Q17.2	Microtia
Q17.3	Other misshapen ear
Q17.4	Misplaced ear
Q17.5	Prominent ear
Q17.8	Other specified congenital malformations of ear
Q17.9	Congenital malformation of ear, unspecified
Q18	Other congenital malformations of face and neck
Q18.0	Sinus, fistula and cyst of branchial cleft
Q18.1	Preauricular sinus and cyst
Q18.2	Other branchial cleft malformations
Q18.3	Webbing of neck
Q18.4	Macrostomia
Q18.5	Microstomia
Q18.6	Macrocheilia
Q18.7	Microcheilia
Q18.8	Other specified congenital malformations of face and neck
Q18.9	Congenital malformation of face and neck, unspecified
Q20	Congenital malformations of cardiac chambers and connections
Q20.0	Common arterial trunk
Q20.1	Double outlet right ventricle
Q20.2	Double outlet left ventricle
Q20.3	Discordant ventriculoarterial connection
Q20.4	Double inlet ventricle
Q20.5	Discordant atrioventricular connection
Q20.6	Isomerism of atrial appendages
Q20.8	Other congenital malformations of cardiac chambers and connections
Q20.9	Congenital malformation of cardiac chambers and connections,unspecified
Q21	Congenital malformations of cardiac septa
Q21.0	Ventricular septal defect
Q21.1	Atrial septal defect
Q21.2	Atrioventricular septal defect
Q21.3	Tetralogy of Fallot
Q21.4	Aortopulmonary septal defect
Q21.8	Other congenital malformations of cardiac septa
Q21.9	Congenital malformation of cardiac septum, unspecified
Q22	Congenital malformations of pulmonary and tricuspid valves
Q22.0	Pulmonary valve atresia
Q22.1	Congenital pulmonary valve stenosis
Q22.2	Congenital pulmonary valve insufficiency
Q22.3	Other congenital malformations of pulmonary valve
Q22.4	Congenital tricuspid stenosis
Q22.5	Ebstein's anomaly
Q22.6	Hypoplastic right heart syndrome
Q22.8	Other congenital malformations of tricuspid valve
Q22.9	Congenital malformation of tricuspid valve, unspecified
Q23	Congenital malformations of aortic and mitral valves
Q23.0	Congenital stenosis of aortic valve
Q23.1	Congenital insufficiency of aortic valve
Q23.2	Congenital mitral stenosis
Q23.3	Congenital mitral insufficiency
Q23.4	Hypoplastic left heart syndrome
Q23.8	Other congenital malformations of aortic and mitral valves
Q23.9	Congenital malformation of aortic and mitral valves, unspecified
Q24	Other congenital malformations of heart
Q24.0	Dextrocardia
Q24.1	Laevocardia
Q24.2	Cor triatriatum
Q24.3	Pulmonary infundibular stenosis
Q24.4	Congenital subaortic stenosis
Q24.5	Malformation of coronary vessels
Q24.6	Congenital heart block
Q24.8	Other specified congenital malformations of heart
Q24.9	Congenital malformation of heart, unspecified
Q25	Congenital malformations of great arteries
Q25.0	Patent ductus arteriosus
Q25.1	Coarctation of aorta
Q25.2	Atresia of aorta
Q25.3	Stenosis of aorta
Q25.4	Other congenital malformations of aorta
Q25.5	Atresia of pulmonary artery
Q25.6	Stenosis of pulmonary artery
Q25.7	Other congenital malformations of pulmonary artery
Q25.8	Other congenital malformations of great arteries
Q25.9	Congenital malformation of great arteries, unspecified
Q26	Congenital malformations of great veins
Q26.0	Congenital stenosis of vena cava
Q26.1	Persistent left superior vena cava
Q26.2	Total anomalous pulmonary venous connection
Q26.3	Partial anomalous pulmonary venous connection
Q26.4	Anomalous pulmonary venous connection, unspecified
Q26.5	Anomalous portal venous connection
Q26.6	Portal vein-hepatic artery fistula
Q26.8	Other congenital malformations of great veins
Q26.9	Congenital malformation of great vein, unspecified
Q27	Other congenital malformations of peripheral vascular system
Q27.0	Congenital absence and hypoplasia of umbilical artery
Q27.1	Congenital renal artery stenosis
Q27.2	Other congenital malformations of renal artery
Q27.3	Peripheral arteriovenous malformation
Q27.4	Congenital phlebectasia
Q27.8	Other specified congenital malformations of peripheral vascularsystem
Q27.9	Congenital malformation of peripheral vascular system, unspecified
Q28	Other congenital malformations of circulatory system
Q28.0	Arteriovenous malformation of precerebral vessels
Q28.1	Other malformations of precerebral vessels
Q28.2	Arteriovenous malformation of cerebral vessels
Q28.3	Other malformations of cerebral vessels
Q28.8	Other specified congenital malformations of circulatory system
Q28.9	Congenital malformation of circulatory system, unspecified
Q30	Congenital malformations of nose
Q30.0	Choanal atresia
Q30.1	Agenesis and underdevelopment of nose
Q30.2	Fissured, notched and cleft nose
Q30.3	Congenital perforated nasal septum
Q30.8	Other congenital malformations of nose
Q30.9	Congenital malformation of nose, unspecified
Q31	Congenital malformations of larynx
Q31.0	Web of larynx
Q31.1	Congenital subglottic stenosis
Q31.2	Laryngeal hypoplasia
Q31.3	Laryngocele
Q31.4	Congenital laryngeal stridor
Q31.8	Other congenital malformations of larynx
Q31.9	Congenital malformation of larynx, unspecified
Q32	Congenital malformations of trachea and bronchus
Q32.0	Congenital tracheomalacia
Q32.1	Other congenital malformations of trachea
Q32.2	Congenital bronchomalacia
Q32.3	Congenital stenosis of bronchus
Q32.4	Other congenital malformations of bronchus
Q33	Congenital malformations of lung
Q33.0	Congenital cystic lung
Q33.1	Accessory lobe of lung
Q33.2	Sequestration of lung
Q33.3	Agenesis of lung
Q33.4	Congenital bronchiectasis
Q33.5	Ectopic tissue in lung
Q33.6	Hypoplasia and dysplasia of lung
Q33.8	Other congenital malformations of lung
Q33.9	Congenital malformation of lung, unspecified
Q34	Other congenital malformations of respiratory system
Q34.0	Anomaly of pleura
Q34.1	Congenital cyst of mediastinum
Q34.8	Other specified congenital malformations of respiratory system
Q34.9	Congenital malformation of respiratory system, unspecified
Q35	Cleft palate
Q35.0	Cleft hard palate, bilateral
Q35.1	Cleft hard palate, unilateral
Q35.2	Cleft soft palate, bilateral
Q35.3	Cleft soft palate, unilateral
Q35.4	Cleft hard palate with cleft soft palate, bilateral
Q35.5	Cleft hard palate with cleft soft palate, unilateral
Q35.6	Cleft palate, medial
Q35.7	Cleft uvula
Q35.8	Cleft palate, unspecified, bilateral
Q35.9	Cleft palate, unspecified, unilateral
Q36	Cleft lip
Q36.0	Cleft lip, bilateral
Q36.1	Cleft lip, medial
Q36.9	Cleft lip, unilateral
Q37	Cleft palate with cleft lip
Q37.0	Cleft hard palate with cleft lip, bilateral
Q37.1	Cleft hard palate with cleft lip, unilateral
Q37.2	Cleft soft palate with cleft lip, bilateral
Q37.3	Cleft soft palate with cleft lip, unilateral
Q37.4	Cleft hard and soft palate with cleft lip, bilateral
Q37.5	Cleft hard and soft palate with cleft lip, unilateral
Q37.8	Unspecified cleft palate with cleft lip, bilateral
Q37.9	Unspecified cleft palate with cleft lip, unilateral
Q38	Other congenital malformations of tongue, mouth and pharynx
Q38.0	Congenital malformations of lips, not elsewhere classified
Q38.1	Ankyloglossia
Q38.2	Macroglossia
Q38.3	Other congenital malformations of tongue
Q38.4	Congenital malformations of salivary glands and ducts
Q38.5	Congenital malformations of palate, not elsewhere classified
Q38.6	Other congenital malformations of mouth
Q38.7	Pharyngeal pouch
Q38.8	Other congenital malformations of pharynx
Q39	Congenital malformations of oesophagus
Q39.0	Atresia of oesophagus without fistula
Q39.1	Atresia of oesophagus with tracheo-oesophageal fistula
Q39.2	Congenital tracheo-oesophageal fistula without atresia
Q39.3	Congenital stenosis and stricture of oesophagus
Q39.4	Oesophageal web
Q39.5	Congenital dilatation of oesophagus
Q39.6	Diverticulum of oesophagus
Q39.8	Other congenital malformations of oesophagus
Q39.9	Congenital malformation of oesophagus, unspecified
Q40	Other congenital malformations of upper alimentary tract
Q40.0	Congenital hypertrophic pyloric stenosis
Q40.1	Congenital hiatus hernia
Q40.2	Other specified congenital malformations of stomach
Q40.3	Congenital malformation of stomach, unspecified
Q40.8	Other specified congenital malformations of upper alimentary tract
Q40.9	Congenital malformation of upper alimentary tract, unspecified
Q41	Congenital absence, atresia and stenosis of small intestine
Q41.0	Congenital absence, atresia and stenosis of duodenum
Q41.1	Congenital absence, atresia and stenosis of jejunum
Q41.2	Congenital absence, atresia and stenosis of ileum
Q41.8	Congenital absence, atresia and stenosis of other specified parts ofsmall intestine
Q41.9	Congenital absence, atresia and stenosis of small intestine, partunspecified
Q42	Congenital absence, atresia and stenosis of large intestine
Q42.0	Congenital absence, atresia and stenosis of rectum with fistula
Q42.1	Congenital absence, atresia and stenosis of rectum without fistula
Q42.2	Congenital absence, atresia and stenosis of anus with fistula
Q42.3	Congenital absence, atresia and stenosis of anus without fistula
Q42.8	Congenital absence, atresia and stenosis of other parts of largeintestine
Q42.9	Congenital absence, atresia and stenosis of large intestine, partunspecified
Q43	Other congenital malformations of intestine
Q43.0	Meckel's diverticulum
Q43.1	Hirschsprung's disease
Q43.2	Other congenital functional disorders of colon
Q43.3	Congenital malformations of intestinal fixation
Q43.4	Duplication of intestine
Q43.5	Ectopic anus
Q43.6	Congenital fistula of rectum and anus
Q43.7	Persistent cloaca
Q43.8	Other specified congenital malformations of intestine
Q43.9	Congenital malformation of intestine, unspecified
Q44	Congenital malformations of gallbladder, bile ducts and liver
Q44.0	Agenesis, aplasia and hypoplasia of gallbladder
Q44.1	Other congenital malformations of gallbladder
Q44.2	Atresia of bile ducts
Q44.3	Congenital stenosis and stricture of bile ducts
Q44.4	Choledochal cyst
Q44.5	Other congenital malformations of bile ducts
Q44.6	Cystic disease of liver
Q44.7	Other congenital malformations of liver
Q45	Other congenital malformations of digestive system
Q45.0	Agenesis, aplasia and hypoplasia of pancreas
Q45.1	Annular pancreas
Q45.2	Congenital pancreatic cyst
Q45.3	Other congenital malformations of pancreas and pancreatic duct
Q45.8	Other specified congenital malformations of digestive system
Q45.9	Congenital malformation of digestive system, unspecified
Q50	Congenital malformations of ovaries, fallopian tubes and broadligaments
Q50.0	Congenital absence of ovary
Q50.1	Developmental ovarian cyst
Q50.2	Congenital torsion of ovary
Q50.3	Other congenital malformations of ovary
Q50.4	Embryonic cyst of fallopian tube
Q50.5	Embryonic cyst of broad ligament
Q50.6	Other congenital malformations of fallopian tube and broad ligament
Q51	Congenital malformations of uterus and cervix
Q51.0	Agenesis and aplasia of uterus
Q51.1	Doubling of uterus with doubling of cervix and vagina
Q51.2	Other doubling of uterus
Q51.3	Bicornate uterus
Q51.4	Unicornate uterus
Q51.5	Agenesis and aplasia of cervix
Q51.6	Embryonic cyst of cervix
Q51.7	Congenital fistulae between uterus and digestive and urinary tracts
Q51.8	Other congenital malformations of uterus and cervix
Q51.9	Congenital malformation of uterus and cervix, unspecified
Q52	Other congenital malformations of female genitalia
Q52.0	Congenital absence of vagina
Q52.1	Doubling of vagina
Q52.2	Congenital rectovaginal fistula
Q52.3	Imperforate hymen
Q52.4	Other congenital malformations of vagina
Q52.5	Fusion of labia
Q52.6	Congenital malformation of clitoris
Q52.7	Other congenital malformations of vulva
Q52.8	Other specified congenital malformations of female genitalia
Q52.9	Congenital malformation of female genitalia, unspecified
Q53	Undescended testicle
Q53.0	Ectopic testis
Q53.1	Undescended testicle, unilateral
Q53.2	Undescended testicle, bilateral
Q53.9	Undescended testicle, unspecified
Q54	Hypospadias
Q54.0	Hypospadias, balanic
Q54.1	Hypospadias, penile
Q54.2	Hypospadias, penoscrotal
Q54.3	Hypospadias, perineal
Q54.4	Congenital chordee
Q54.8	Other hypospadias
Q54.9	Hypospadias, unspecified
Q55	Other congenital malformations of male genital organs
Q55.0	Absence and aplasia of testis
Q55.1	Hypoplasia of testis and scrotum
Q55.2	Other congenital malformations of testis and scrotum
Q55.3	Atresia of vas deferens
Q55.4	Other congenital malformations of vas deferens, epididymis, seminalvesicles and prostate
Q55.5	Congenital absence and aplasia of penis
Q55.6	Other congenital malformations of penis
Q55.8	Other specified congenital malformations of male genital organs
Q55.9	Congenital malformation of male genital organ, unspecified
Q56	Indeterminate sex and pseudohermaphroditism
Q56.0	Hermaphroditism, not elsewhere classified
Q56.1	Male pseudohermaphroditism, not elsewhere classified
Q56.2	Female pseudohermaphroditism, not elsewhere classified
Q56.3	Pseudohermaphroditism, unspecified
Q56.4	Indeterminate sex, unspecified
Q60	Renal agenesis and other reduction defects of kidney
Q60.0	Renal agenesis, unilateral
Q60.1	Renal agenesis, bilateral
Q60.2	Renal agenesis, unspecified
Q60.3	Renal hypoplasia, unilateral
Q60.4	Renal hypoplasia, bilateral
Q60.5	Renal hypoplasia, unspecified
Q60.6	Potter's syndrome
Q61	Cystic kidney disease
Q61.0	Congenital single renal cyst
Q61.1	Polycystic kidney, infantile type
Q61.2	Polycystic kidney, adult type
Q61.3	Polycystic kidney, unspecified
Q61.4	Renal dysplasia
Q61.5	Medullary cystic kidney
Q61.8	Other cystic kidney diseases
Q61.9	Cystic kidney disease, unspecified
Q62	Congenital obstructive defects of renal pelvis and congenitalmalformations of ureter
Q62.0	Congenital hydronephrosis
Q62.1	Atresia and stenosis of ureter
Q62.2	Congenital megaloureter
Q62.3	Other obstructive defects of renal pelvis and ureter
Q62.4	Agenesis of ureter
Q62.5	Duplication of ureter
Q62.6	Malposition of ureter
Q62.7	Congenital vesico-uretero-renal reflux
Q62.8	Other congenital malformations of ureter
Q63	Other congenital malformations of kidney
Q63.0	Accessory kidney
Q63.1	Lobulated, fused and horseshoe kidney
Q63.2	Ectopic kidney
Q63.3	Hyperplastic and giant kidney
Q63.8	Other specified congenital malformations of kidney
Q63.9	Congenital malformation of kidney, unspecified
Q64	Other congenital malformations of urinary system
Q64.0	Epispadias
Q64.1	Exstrophy of urinary bladder
Q64.2	Congenital posterior urethral valves
Q64.3	Other atresia and stenosis of urethra and bladder neck
Q64.4	Malformation of urachus
Q64.5	Congenital absence of bladder and urethra
Q64.6	Congenital diverticulum of bladder
Q64.7	Other congenital malformations of bladder and urethra
Q64.8	Other specified congenital malformations of urinary system
Q64.9	Congenital malformation of urinary system, unspecified
Q65	Congenital deformities of hip
Q65.0	Congenital dislocation of hip, unilateral
Q65.1	Congenital dislocation of hip, bilateral
Q65.2	Congenital dislocation of hip, unspecified
Q65.3	Congenital subluxation of hip, unilateral
Q65.4	Congenital subluxation of hip, bilateral
Q65.5	Congenital subluxation of hip, unspecified
Q65.6	Unstable hip
Q65.8	Other congenital deformities of hip
Q65.9	Congenital deformity of hip, unspecified
Q66	Congenital deformities of feet
Q66.0	Talipes equinovarus
Q66.1	Talipes calcaneovarus
Q66.2	Metatarsus varus
Q66.3	Other congenital varus deformities of feet
Q66.4	Talipes calcaneovalgus
Q66.5	Congenital pes planus
Q66.6	Other congenital valgus deformities of feet
Q66.7	Pes cavus
Q66.8	Other congenital deformities of feet
Q66.9	Congenital deformity of feet, unspecified
Q67	Congenital musculoskeletal deformities of head, face, spine andchest
Q67.0	Facial asymmetry
Q67.1	Compression facies
Q67.2	Dolichocephaly
Q67.3	Plagiocephaly
Q67.4	Other congenital deformities of skull, face and jaw
Q67.5	Congenital deformity of spine
Q67.6	Pectus excavatum
Q67.7	Pectus carinatum
Q67.8	Other congenital deformities of chest
Q68	Other congenital musculoskeletal deformities
Q68.0	Congenital deformity of sternocleidomastoid muscle
Q68.1	Congenital deformity of hand
Q68.2	Congenital deformity of knee
Q68.3	Congenital bowing of femur
Q68.4	Congenital bowing of tibia and fibula
Q68.5	Congenital bowing of long bones of leg, unspecified
Q68.8	Other specified congenital musculoskeletal deformities
Q69	Polydactyly
Q69.0	Accessory finger(s)
Q69.1	Accessory thumb(s)
Q69.2	Accessory toe(s)
Q69.9	Polydactyly, unspecified
Q70	Syndactyly
Q70.0	Fused fingers
Q70.1	Webbed fingers
Q70.2	Fused toes
Q70.3	Webbed toes
Q70.4	Polysyndactyly
Q70.9	Syndactyly, unspecified
Q71	Reduction defects of upper limb
Q71.0	Congenital complete absence of upper limb(s)
Q71.1	Congenital absence of upper arm and forearm with hand present
Q71.2	Congenital absence of both forearm and hand
Q71.3	Congenital absence of hand and finger(s)
Q71.4	Longitudinal reduction defect of radius
Q71.5	Longitudinal reduction defect of ulna
Q71.6	Lobster-claw hand
Q71.8	Other reduction defects of upper limb(s)
Q71.9	Reduction defect of upper limb, unspecified
Q72	Reduction defects of lower limb
Q72.0	Congenital complete absence of lower limb(s)
Q72.1	Congenital absence of thigh and lower leg with foot present
Q72.2	Congenital absence of both lower leg and foot
Q72.3	Congenital absence of foot and toe(s)
Q72.4	Longitudinal reduction defect of femur
Q72.5	Longitudinal reduction defect of tibia
Q72.6	Longitudinal reduction defect of fibula
Q72.7	Split foot
Q72.8	Other reduction defects of lower limb(s)
Q72.9	Reduction defect of lower limb, unspecified
Q73	Reduction defects of unspecified limb
Q73.0	Congenital absence of unspecified limb(s)
Q73.1	Phocomelia, unspecified limb(s)
Q73.8	Other reduction defects of unspecified limb(s)
Q74	Other congenital malformations of limb(s)
Q74.0	Other congenital malformations of upper limb(s), including shouldergirdle
Q74.1	Congenital malformation of knee
Q74.2	Other congenital malformations of lower limb(s), including pelvicgirdle
Q74.3	Arthrogryposis multiplex congenita
Q74.8	Other specified congenital malformations of limb(s)
Q74.9	Unspecified congenital malformation of limb(s)
Q75	Other congenital malformations of skull and face bones
Q75.0	Craniosynostosis
Q75.1	Craniofacial dysostosis
Q75.2	Hypertelorism
Q75.3	Macrocephaly
Q75.4	Mandibulofacial dysostosis
Q75.5	Oculomandibular dysostosis
Q75.8	Other specified congenital malformations of skull and face bones
Q75.9	Congenital malformation of skull and face bones, unspecified
Q76	Congenital malformations of spine and bony thorax
Q76.0	Spina bifida occulta
Q76.1	Klippel-Feil syndrome
Q76.2	Congenital spondylolisthesis
Q76.3	Congenital scoliosis due to congenital bony malformation
Q76.4	Other congenital malformations of spine, not associated withscoliosis
Q76.5	Cervical rib
Q76.6	Other congenital malformations of ribs
Q76.7	Congenital malformation of sternum
Q76.8	Other congenital malformations of bony thorax
Q76.9	Congenital malformation of bony thorax, unspecified
Q77	Osteochondrodysplasia with defects of growth of tubular bones andspine
Q77.0	Achondrogenesis
Q77.1	Thanatophoric short stature
Q77.2	Short rib syndrome
Q77.3	Chondrodysplasia punctata
Q77.4	Achondroplasia
Q77.5	Dystrophic dysplasia
Q77.6	Chondroectodermal dysplasia
Q77.7	Spondyloepiphyseal dysplasia
Q77.8	Other osteochondrodysplasia with defects of growth of tubular bonesand spine
Q77.9	Osteochondrodysplasia with defects of growth of tubular bones andspine, unspecified
Q78	Other osteochondrodysplasias
Q78.0	Osteogenesis imperfecta
Q78.1	Polyostotic fibrous dysplasia
Q78.2	Osteopetrosis
Q78.3	Progressive diaphyseal dysplasia
Q78.4	Enchondromatosis
Q78.5	Metaphyseal dysplasia
Q78.6	Multiple congenital exostoses
Q78.8	Other specified osteochondrodysplasias
Q78.9	Osteochondrodysplasia, unspecified
Q79	Congenital malformations of the musculoskeletal system, notelsewhere classified
Q79.0	Congenital diaphragmatic hernia
Q79.1	Other congenital malformations of diaphragm
Q79.2	Exomphalos
Q79.3	Gastroschisis
Q79.4	Prune belly syndrome
Q79.5	Other congenital malformations of abdominal wall
Q79.6	Ehlers-Danlos syndrome
Q79.8	Other congenital malformations of musculoskeletal system
Q79.9	Congenital malformation of musculoskeletal system, unspecified
Q80	Congenital ichthyosis
Q80.0	Ichthyosis vulgaris
Q80.1	X-linked ichthyosis
Q80.2	Lamellar ichthyosis
Q80.3	Congenital bullous ichthyosiform erythroderma
Q80.4	Harlequin fetus
Q80.8	Other congenital ichthyosis
Q80.9	Congenital ichthyosis, unspecified
Q81	Epidermolysis bullosa
Q81.0	Epidermolysis bullosa simplex
Q81.1	Epidermolysis bullosa letalis
Q81.2	Epidermolysis bullosa dystrophica
Q81.8	Other epidermolysis bullosa
Q81.9	Epidermolysis bullosa, unspecified
Q82	Other congenital malformations of skin
Q82.0	Hereditary lymphoedema
Q82.1	Xeroderma pigmentosum
Q82.2	Mastocytosis
Q82.3	Incontinentia pigmenti
Q82.4	Ectodermal dysplasia (anhidrotic)
Q82.5	Congenital non-neoplastic naevus
Q82.8	Other specified congenital malformations of skin
Q82.9	Congenital malformation of skin, unspecified
Q83	Congenital malformations of breast
Q83.0	Congenital absence of breast with absent nipple
Q83.1	Accessory breast
Q83.2	Absent nipple
Q83.3	Accessory nipple
Q83.8	Other congenital malformations of breast
Q83.9	Congenital malformation of breast, unspecified
Q84	Other congenital malformations of integument
Q84.0	Congenital alopecia
Q84.1	Congenital morphological disturbances of hair, not elsewhereclassified
Q84.2	Other congenital malformations of hair
Q84.3	Anonychia
Q84.4	Congenital leukonychia
Q84.5	Enlarged and hypertrophic nails
Q84.6	Other congenital malformations of nails
Q84.8	Other specified congenital malformations of integument
Q84.9	Congenital malformation of integument, unspecified
Q85	Phakomatoses, not elsewhere classified
Q85.0	Neurofibromatosis (nonmalignant)
Q85.1	Tuberous sclerosis
Q85.8	Other phakomatoses, not elsewhere classified
Q85.9	Phakomatosis, unspecified
Q86	Congenital malformation syndromes due to known exogenous causes, notelsewhere classified
Q86.0	Fetal alcohol syndrome (dysmorphic)
Q86.1	Fetal hydantoin syndrome
Q86.2	Dysmorphism due to warfarin
Q86.8	Other congenital malformation syndromes due to known exogenouscauses
Q87	Other specified congenital malformation syndromes affecting multiplesystems
Q87.0	Congenital malformation syndromes predominantly affecting facialappearance
Q87.1	Congenital malformation syndromes predominantly associated withshort stature
Q87.2	Congenital malformation syndromes predominantly involving limbs
Q87.3	Congenital malformation syndromes involving early overgrowth
Q87.4	Marfan's syndrome
Q87.5	Other congenital malformation syndromes with other skeletal changes
Q87.8	Other specified congenital malformation syndromes, not elsewhereclassified
Q89	Other congenital malformations, not elsewhere classified
Q89.0	Congenital malformations of spleen
Q89.1	Congenital malformations of adrenal gland
Q89.2	Congenital malformations of other endocrine glands
Q89.3	Situs inversus
Q89.4	Conjoined twins
Q89.7	Multiple congenital malformations, not elsewhere classified
Q89.8	Other specified congenital malformations
Q89.9	Congenital malformation, unspecified
Q90	Down's syndrome
Q90.0	Trisomy 21, meiotic nondisjunction
Q90.1	Trisomy 21, mosaicism (mitotic nondisjunction)
Q90.2	Trisomy 21, translocation
Q90.9	Down's syndrome, unspecified
Q91	Edwards' syndrome and Patau's syndrome
Q91.0	Trisomy 18, meiotic nondisjunction
Q91.1	Trisomy 18, mosaicism (mitotic nondisjunction)
Q91.2	Trisomy 18, translocation
Q91.3	Edwards' syndrome, unspecified
Q91.4	Trisomy 13, meiotic nondisjunction
Q91.5	Trisomy 13, mosaicism (mitotic nondisjunction)
Q91.6	Trisomy 13, translocation
Q91.7	Patau's syndrome, unspecified
Q92	Other trisomies and partial trisomies of the autosomes, notelsewhere classified
Q92.0	Whole chromosome trisomy, meiotic nondisjunction
Q92.1	Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
Q92.2	Major partial trisomy
Q92.3	Minor partial trisomy
Q92.4	Duplications seen only at prometaphase
Q92.5	Duplications with other complex rearrangements
Q92.6	Extra marker chromosomes
Q92.7	Triploidy and polyploidy
Q92.8	Other specified trisomies and partial trisomies of autosomes
Q92.9	Trisomy and partial trisomy of autosomes, unspecified
Q93	Monosomies and deletions from the autosomes, not elsewhereclassified
Q93.0	Whole chromosome monosomy, meiotic nondisjunction
Q93.1	Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
Q93.2	Chromosome replaced with ring or dicentric
Q93.3	Deletion of short arm of chromosome 4
Q93.4	Deletion of short arm of chromosome 5
Q93.5	Other deletions of part of a chromosome
Q93.6	Deletions seen only at prometaphase
Q93.7	Deletions with other complex rearrangements
Q93.8	Other deletions from the autosomes
Q93.9	Deletion from autosomes, unspecified
Q95	Balanced rearrangements and structural markers, not elsewhereclassified
Q95.0	Balanced translocation and insertion in normal individual
Q95.1	Chromosome inversion in normal individual
Q95.2	Balanced autosomal rearrangement in abnormal individual
Q95.3	Balanced sex/autosomal rearrangement in abnormal individual
Q95.4	Individuals with marker heterochromatin
Q95.5	Individuals with autosomal fragile site
Q95.8	Other balanced rearrangements and structural markers
Q95.9	Balanced rearrangement and structural marker, unspecified
Q96	Turner's syndrome
Q96.0	Karyotype 45,X
Q96.1	Karyotype 46,X iso (Xq)
Q96.2	Karyotype 46,X with abnormal sex chromosome, except iso (Xq)
Q96.3	Mosaicism, 45,X/46,XX or XY
Q96.4	Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome
Q96.8	Other variants of Turner's syndrome
Q96.9	Turner's syndrome, unspecified
Q97	Other sex chromosome abnormalities, female phenotype, not elsewhereclassified
Q97.0	Karyotype 47,XXX
Q97.1	Female with more than three X chromosomes
Q97.2	Mosaicism, lines with various numbers of X chromosomes
Q97.3	Female with 46,XY karyotype
Q97.8	Other specified sex chromosome abnormalities, female phenotype
Q97.9	Sex chromosome abnormality, female phenotype, unspecified
Q98	Other sex chromosome abnormalities, male phenotype, not elsewhereclassified
Q98.0	Klinefelter's syndrome karyotype 47,XXY
Q98.1	Klinefelter's syndrome, male with more than two X chromosomes
Q98.2	Klinefelter's syndrome, male with 46,XX karyotype
Q98.3	Other male with 46,XX karyotype
Q98.4	Klinefelter's syndrome, unspecified
Q98.5	Karyotype 47,XYY
Q98.6	Male with structurally abnormal sex chromosome
Q98.7	Male with sex chromosome mosaicism
Q98.8	Other specified sex chromosome abnormalities, male phenotype
Q98.9	Sex chromosome abnormality, male phenotype, unspecified
Q99	Other chromosome abnormalities, not elsewhere classified
Q99.0	Chimera 46,XX/46,XY
Q99.1	46,XX true hermaphrodite
Q99.2	Fragile X chromosome
Q99.8	Other specified chromosome abnormalities
Q99.9	Chromosomal abnormality, unspecified