Disease #05053 (MCCRP3 (microcephaly and chorioretinopathy, autosomal recessive, type 3 (MCCRP-3)), OMIM:616335)

Official abbreviation	MCCRP3
Name	microcephaly and chorioretinopathy, autosomal recessive, type 3 (MCCRP-3)
OMIM ID	616335
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TUBGCP4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD