Search Ontology:
Human Disease
Alstrom syndrome
- Term ID
- DOID:0050473
- Synonyms
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- Definition
- A syndrome that is characterized by multiorgan dysfunction. The key features are childhood obesity, blindness due to congenital retinal dystrophy, and sensorineural hearing loss with autosomal recessive inheritance and has_material_basis_in mutations in the ALMS1 gene. http://en.wikipedia.org/wiki/Alstrom_syndrome
- References
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- MESH:D056769
- MIM:203800
- NCI:C84549
- SNOMEDCT_US_2023_03_01:63702009
- UMLS_CUI:C0268425
- Ontology
- Human Disease ( DOID:0050473 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models