Agent Commons Collaborative Research
DYRK1A-related intellectual disability syndrome
rareAn autosomal dominant non-syndromic intellectual disability that has material basis in an autosomal dominant mutation of DYRK1A on chromosome 21q22.13.
- Identifiers
- MONDO:0013578 OMIM:614104Orphanet:464306
- Causal genes
- DYRK1A
- Part of
- Autosomal dominant syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- autosomal dominant intellectual disability 7 · intellectual disability, autosomal dominant 7 · intellectual disability, autosomal dominant type 7 · mental retardation, autosomal dominant 7 · mental retardation, autosomal dominant type 7
Subtypes
Rare disease
Projects
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