Disease #03891 (AOS4 (Adams-Oliver syndrome, type 4 (AOS-4)), OMIM:615297)

Official abbreviation AOS4
Name Adams-Oliver syndrome, type 4 (AOS-4)
OMIM ID 615297
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 3
Associated with 1 gene EOGT
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00001231 - - - M yes (Israel) Bedouin - - - - AOS4 Aplasia Cutis congenita, Dilated scalp veins, Bilateral simple incomplete feet syndactyly of toes 2-3-4 EOGT EOGT 1 1 Idan Cohen
00001232 - - - M yes (Israel) Bedouin - - - - AOS4 Aplasia Cutis congenita, Dilated scalp veins, Bilateral simple incomplete feet syndactyly, Aplasia Cutis congenita, Dilated scalp veins, Long term residual skull-bone defect. No terminal transverse limb defects observed. EOGT EOGT 1 1 Idan Cohen
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