Disease #00113 (FFDD3 (dysplasia, dermal, focal facial, type 3 (FFDD-3, Setleis)), OMIM:227260)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FFDD3
Name	dysplasia, dermal, focal facial, type 3 (FFDD-3, Setleis)
OMIM ID	227260
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	3
Associated with 1 gene	TWIST2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-02-21 17:15:35 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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