Disease #04592 (LSDMCA3 (skin defects, linear, with multiple congenital anomalies, type 3 (LSDMCA-3)), OMIM:300952)

Official abbreviation	LSDMCA3
Name	skin defects, linear, with multiple congenital anomalies, type 3 (LSDMCA-3)
OMIM ID	300952
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NDUFB11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD