Search Ontology:
Human Disease
neurodevelopmental disorder with poor growth, seizures, and brain abnormalities
- Term ID
- DOID:0070814
- Synonyms
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- NEDGSB
- 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. https://pubmed.ncbi.nlm.nih.gov/39962046/
- References
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- MIM:621154
- UMLS_CUI:C6012710
- Ontology
- Human Disease ( DOID:0070814 )
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Genes Involved
Zebrafish Models