Malformatii congenitale, deformatii si anomalii cromozomiale
Malformatii congenitale, deformatii si anomalii cromozomiale
Malformatii congenitale, deformatii si anomalii cromozomiale
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<strong>Malformatii</strong> <strong>congenitale</strong>, <strong>deformatii</strong> <strong>si</strong> <strong>anomalii</strong> <strong>cromozomiale</strong><br />
Q86.84 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />
agentilor citotoxici<br />
Q86.85 <strong>Malformatii</strong> <strong>congenitale</strong> datorite altor<br />
medicamente<br />
Exclude: dismorfism datorit warfarinei<br />
(Q86.2)<br />
Q86.86 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />
radiatiilor ionizante<br />
Q86.87 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />
metililor mercurului<br />
Q86.89 <strong>Malformatii</strong> <strong>congenitale</strong> datorite<br />
cauzelor exogene specificate<br />
Q87 Alte <strong>si</strong>ndroame de malformatii<br />
<strong>congenitale</strong> specificate afectand<br />
<strong>si</strong>steme multiple<br />
Q87.0 Sindroame de malformatii <strong>congenitale</strong><br />
afectand in special fizionomia fetei<br />
Q87.01 Acrocefalopoli<strong>si</strong>ndactilia<br />
Acrocefalopoli<strong>si</strong>ndactilia tip I, <strong>si</strong>ndromul<br />
Noack<br />
Acrocefalopoli<strong>si</strong>ndactilia tip II,<br />
<strong>si</strong>ndromul Carpenter<br />
Q87.02 Acrocefalo<strong>si</strong>ndactilia<br />
Sindromul Apert<br />
Cefalodactilia Vogt<br />
Q87.03 Sindromul criptoftalmic<br />
Sindromul Fraser<br />
Q87.04 Sindromul Treacher Collins<br />
[-Franceschetti] [-Klein]<br />
Exclude: disostoza mandibulo-faciala<br />
producandu-se ca o<br />
anomalie izolata (Q75.4)<br />
Q87.05 Sindromul Hallerman-Streiff<br />
Exclude: disostoza oculo-mandibulara<br />
producandu-se ca o<br />
anomalie izolata (Q75.5)<br />
Q87.06 Episodul Pierre Robin<br />
Sindromul <strong>si</strong> episodul Robin<br />
Q87.07 Sindromul Pena-Shokeir<br />
Sindromul hipoplaziei pulmonare cu<br />
<strong>anomalii</strong> faciale anchilozante<br />
camptodactile<br />
368<br />
Q87.09 Alte <strong>si</strong>ndroame de malformatii<br />
<strong>congenitale</strong> afectand in special<br />
fizionomia fetei<br />
Sindrom de malformatii <strong>congenitale</strong><br />
afectand in special fizionomia fetei NOS<br />
Ciclopia [ciclop][ciclopism][<strong>si</strong>noftalmia]<br />
Discraniopigofalangism<br />
Artro-oftalmia progre<strong>si</strong>va ereditara<br />
Sindrom:<br />
- Goldenhar<br />
- Moebius<br />
- Mohr<br />
- oculo-auriculo-vertebral [microzomia<br />
hemifaciala]<br />
- orofacial-digital tip I <strong>si</strong> I<br />
- Stickler<br />
- trico-rino-falangian tip I <strong>si</strong> II [Langer-<br />
Giedion]<br />
- Ullrich-Feichtiger<br />
- fizionomia Whistling<br />
Exclude: cherubism (K10.8)<br />
<strong>si</strong>ndromul Waardenburg<br />
(E70.3)<br />
Q87.1 Sindroame de malformatii <strong>congenitale</strong><br />
asociate in special cu statura scurta<br />
Exclude: <strong>si</strong>ndromul Ellis-van Creveld<br />
(Q77.6)<br />
<strong>si</strong>ndromul Turner(-Ullrich)<br />
(Q96.-)<br />
Q87.11 Sindromul Cockayne<br />
Q87.12 Sindromul Cornelia de Lange<br />
Pitic Amsterdam [<strong>si</strong>ndromul Brachmannde<br />
Lange]<br />
Q87.13 Sindromul Noonan<br />
Afectiune asemanatoare <strong>si</strong>ndromului<br />
Turner<br />
Q87.14 Sindromul Prader-Willi<br />
Q87.15 Sindromul Russell-Silver<br />
Q87.16 Sindromul Seckel<br />
Nanism cu cap de pasare<br />
Nanism primordial microcefalic<br />
Q87.17 Sindromul Smith-Lemli-Opitz<br />
Deficienta de 7-dehidrocolesterol<br />
reductaza<br />
Q87.18 Sindromul Sjogren-Larsson<br />
Alcoolism grasos: deficienta in<br />
nicotinamide adenine dinucleotide<br />
oxidoreductaza<br />
Lista Tabelară a Bolilor ICD-10-AM 2002