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loading...| Preferred Name |
Laurence-Moon Syndrome [Disease/Finding] |
|
| Synonyms |
Laurence-Moon-Biedl Syndrome |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000001790 |
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| altLabel |
Laurence-Moon-Biedl Syndrome Laurence-Moon Syndrome |
|
| cui |
C0023138 |
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| MESH DEFINITION |
An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) |
|
| MESH DUI |
D007849 |
|
| MeSH name |
Laurence-Moon Syndrome |
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| MESH UI |
M0012263 |
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| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000001790 |
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| NUI |
N0000001790 |
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| prefLabel |
Laurence-Moon Syndrome [Disease/Finding] |
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| SNOMED CID |
232059000 |
|
| tui |
T047 |
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| subClassOf |
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