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 -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes FANCB, ZIC3
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Individuals

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00029852 - PubMed: Vetro 2015 - F ? Netherlands - 00y00m02d 0 no - VACTERLX HP:0001511, HP:0002023, HP:0000568, HP:0009777, HP:0003974 FANCL FANCL 1 1 Annalisa Vetro
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