Disease #02482 (CCFDN (cataracts, congenital, facial dysmorphism, and neuropathy (CCFDN)), OMIM:604168)

Official abbreviation	CCFDN
Name	cataracts, congenital, facial dysmorphism, and neuropathy (CCFDN)
OMIM ID	604168
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CTDP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD