Disease #00099 (EDSS1 (dysplasia, ectodermal, syndactyly syndrome, type 1 (EDSS-1)), OMIM:613573)

Global Variome shared LOVD

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Official abbreviation	EDSS1
Name	dysplasia, ectodermal, syndactyly syndrome, type 1 (EDSS-1)
OMIM ID	613573
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PVRL4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-12-14 10:05:44 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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