Disease #05057 (KOS (Kaufman oculocerebrofacial syndrome (KOS)), OMIM:244450)

Official abbreviation KOS
Name Kaufman oculocerebrofacial syndrome (KOS)
OMIM ID 244450
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene UBE3B
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00436806 - - - - - - - - - - - KOS Micrognathia(HP:0000347), Abnormal pinna morphology(HP:0000377), Ventriculomegaly(HP:0002119) - UBE3B 2 1 Yuanyuan Zhou
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