Disease #04493 (ECTDS (dysplasia, ectodermal/short stature syndrome (ECTDS)), OMIM:616029)

Global Variome shared LOVD

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Official abbreviation	ECTDS
Name	dysplasia, ectodermal/short stature syndrome (ECTDS)
OMIM ID	616029
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GRHL2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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