Disease #07043 (MECD1 (dystrophy, corneal, Meesmann, type 1), OMIM:122100)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	MECD1
Name	dystrophy, corneal, Meesmann, type 1
OMIM ID	122100
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KRT12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-11-12 12:00:17 +01:00 (CET)
Date last edited	N/A

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