Disease #06073 (CCAFCA (?Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia), OMIM:616819)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	CCAFCA
Name	?Corpus callosum, agenesis of, with facial anomalies and cerebellar ataxia
OMIM ID	616819
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FRMD4A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.