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neurodevelopmental disorder with poor growth, seizures, and brain abnormalities (DOID:0070814)
Alliance: disease page
Synonyms: NEDGSB
Alt IDs: OMIM:621154, UMLS_CUI:C6012710
Definition: An autosomal recessive intellectual developmental disorder characterized by poor overall growth with short stature and microcephaly, motor and speech delay, and mild-to-severely impaired intellectual development that has_material_basis_in homozygous or compound heterozygous mutation in the SPOUT1 gene on chromosome 9q34.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
09/01/2026
MGI 6.24 		The Jackson Laboratory