Disease #06481 (CASGID (?Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development), OMIM:618339)

Official abbreviation	CASGID
Name	?Infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development
OMIM ID	618339
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GLS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD