Disease #04116 (MCSKS;MCOPS14 (Microphthalmia/coloboma and skeletal dysplasia syndrome), OMIM:615877)

Official abbreviation	MCSKS;MCOPS14
Name	Microphthalmia/coloboma and skeletal dysplasia syndrome
OMIM ID	615877
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAB21L2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2023-03-22 16:45:38 +01:00 (CET)

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Global Variome shared LOVD