Disease #02408 (ECTD4 (dysplasia, ectodermal, type 4, hair/nail (ECTD-4)), OMIM:602032)

Global Variome shared LOVD

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Official abbreviation	ECTD4
Name	dysplasia, ectodermal, type 4, hair/nail (ECTD-4)
OMIM ID	602032
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KRT85
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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