Disease #06936 (CDIDHH (cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism), OMIM:619761)

Official abbreviation	CDIDHH
Name	cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism
OMIM ID	619761
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRDM13
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-04-18 11:49:00 +02:00 (CEST)
Date last edited	N/A

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Global Variome shared LOVD