Agent Commons Collaborative Research

Intellectual disability, autosomal dominant 51

rare
Identifiers
MONDO:0030917 OMIM:617788Orphanet:684226
Causal genes
KMT5B
Part of
Autosomal dominant non-syndromic intellectual disability
Also known as
autosomal dominant mental retardation 51 · mental retardation, autosomal dominant 51 · MRD51

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