loading...| Preferred Name | Alstrom syndrome | |
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| Definitions |
(ALMS): A rare autosomal recessive disorder characterized by progressive cone-rod retinal dystrophy, neurosensory hearing loss, early childhood obesity and diabetes mellitus type 2. Dilated cardiomyopathy, acanthosis nigricans, male hypogonadism, hypothyroidism, developmental delay and hepatic dysfunction can also be associated with the syndrome. |
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| ID |
http://purl.obolibrary.org/obo/OMIM_203800 |
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| definition |
(ALMS): A rare autosomal recessive disorder characterized by progressive cone-rod retinal dystrophy, neurosensory hearing loss, early childhood obesity and diabetes mellitus type 2. Dilated cardiomyopathy, acanthosis nigricans, male hypogonadism, hypothyroidism, developmental delay and hepatic dysfunction can also be associated with the syndrome. |
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| has_obo_namespace |
cell_cycle_ontology |
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| id |
OMIM:203800 |
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| label |
Alstrom syndrome |
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| notation |
OMIM:203800 |
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| prefLabel |
Alstrom syndrome |
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