Metadata | |
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ID | DOID:0070474 |
Name | childhood-onset neurodegeneration with brain atrophy |
Definition | A neurodegenerative disease characterized by loss of motor and cognitive skills between ages 2 and 7 years with progressive cerebral and cerebellar atrophy, resulting in the inability to walk, absence of language, and profound intellectual disability, that has_material_basis_in heterozygous mutation in the UBTF gene on chromosome 17q21.31. https://pubmed.ncbi.nlm.nih.gov/28777933/ |
Xrefs |
SNOMEDCT_US_2023_03_01:1167373005 |
Subsets |
DO_rare_slim |
Synonyms |
childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder [EXACT] CONDBA [EXACT] |
Parent Relationships |