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Human Disease

Alstrom syndrome

Term ID
DOID:0050473
Synonyms
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
Ontology
Human Disease   ( DOID:0050473 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
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