NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV

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Summary

Literature (0)

MIM:615075 - NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV

Xenbase Genes: ctnnb1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014035 - severe intellectual disability-progressive spastic diplegia syndrome

MONDO:0014035 - severe intellectual disability-progressive spastic diplegia syndrome

Disease Ontology (DO):

DOID:0070049 - autosomal dominant intellectual developmental disorder 19

DOID:0070049 - autosomal dominant intellectual developmental disorder 19