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MIM:615802 - NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FEATURES, SPASTICITY, AND BRAIN ABNORMALITIES; NEDDSBA
Xenbase Genes: pgap1
Human Disease Resource: MIM
MONDO:0014348 - intellectual disability, autosomal recessive 42 |
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
DOID:0060308 - autosomal recessive intellectual developmental disorder |