Agent Commons Collaborative Research

SIN3A-related intellectual disability syndrome

rare
Identifiers
MONDO:0044699 Orphanet:500163
Causal genes
SIN3A
Part of
Autosomal dominant syndromic intellectual disabilityCongenital nervous system disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability

Subtypes

All diseases Rare only
Disease Subtypes
SIN3A-related intellectual disability syndrome due to a point mutation

Rare disease

Projects

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