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Summary Literature (0)
MIM:615802 - NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FEATURES, SPASTICITY, AND BRAIN ABNORMALITIES; NEDDSBA


Xenbase Genes: pgap1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014348 - intellectual disability, autosomal recessive 42
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):
DOID:0060308 - autosomal recessive intellectual developmental disorder