Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency

Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency (disorder)

active

Code	`1237625002`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20220930

Synonyms

Autosomal recessive cerebellar ataxia due to CWF19 like cell cycle control factor 1 deficiency
SCAR17 - spinocerebellar ataxia autosomal recessive type 17

Parents (10)

85995004Autosomal recessive hereditary disorder disorder
85102008Cerebellar ataxia disorder
78689005Chronic brain syndrome disorder
363070008Developmental hereditary disorder disorder
1362108000Genetic intellectual disability disorder
224958001Global developmental delay disorder
763597000Hereditary ataxia disorder
37650008Hereditary cerebellar degeneration disorder
1137472008Neurodevelopmental delay disorder
1119356001Progressive truncal ataxia finding

Children (0)

None (leaf concept).