Disease #05951 (COFG (cerebellar, ocular, craniofacial, and genital syndrome (COFG)), OMIM:618479)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	COFG
Name	cerebellar, ocular, craniofacial, and genital syndrome (COFG)
OMIM ID	618479
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAB21L1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-06-28 11:42:50 +02:00 (CEST)
Date last edited	N/A

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