Disease #02270 (VACTERLX (VACTERL association with hydrocephaly, X-linked (VACTERLX)), OMIM:314390)

Official abbreviation VACTERLX
Name VACTERL association with hydrocephaly, X-linked (VACTERLX)
OMIM ID 314390
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes FANCB, ZIC3
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

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00029852 - PubMed: Vetro 2015 - F ? Netherlands - 00y00m02d - no - VACTERLX HP:0001511, HP:0002023, HP:0000568, HP:0009777, HP:0003974 FANCL FANCL 1 1 Annalisa Vetro
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