Disease #01031 (CAASDS (craniofacial anomalies and anterior segment dysgenesis syndrome (CAASDS), OMIM:614195)

Global Variome shared LOVD

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Official abbreviation	CAASDS
Name	craniofacial anomalies and anterior segment dysgenesis syndrome (CAASDS
OMIM ID	614195
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	VSX1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2015-12-08 23:59:30 +01:00 (CET)

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