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neurodevelopmental disorder with white matter abnormalities and gait disturbance (DOID:0070820)
Alliance: disease page
Synonyms: NEDWMG
Alt IDs: OMIM:621152, UMLS_CUI:C6012709
Definition: An autosomal recessive intellectual developmental disorder characterized by macrocephaly, global developmental delay, impaired intellectual development, seizures, behavioral abnormalities, hypotonia, and gait disturbance that has_material_basis_in homozygous or compound heterozygous mutation in the FAM177A1 gene on chromosome 14q13.

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