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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/610156
http://purl.bioontology.org/ontology/OMIM/610156
|
|---|---|
| Preferred Name | IMPAIRED INTELLECTUAL DEVELOPMENT, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME |
| Synonyms |
MORM SYNDROME
MORMS
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MORM SYNDROME
MORMS
MENTAL RETARDATION, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME
|
|---|---|
| prefLabel | IMPAIRED INTELLECTUAL DEVELOPMENT, TRUNCAL OBESITY, RETINAL DYSTROPHY, AND MICROPENIS SYNDROME
|
| Gene Symbol |
MORMS
CORS1
INPP5E
JBTS1
|
| Scope Statement | Caused by mutation in the inositol polyphosphate-5-phosphatase, 72-kd gene (INPP5E, 613037.0001). [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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| tui | T047
|
| Gene Locus | 9q34.3
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| MIMTYPEMEANING | Phenotype description, molecular basis known.
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| notation | 610156
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| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1857802
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| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
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| Delete | Subject | Author | Type | Created |
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| No notes to display |