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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/300997
http://purl.bioontology.org/ontology/OMIM/300997
|
|---|---|
| Preferred Name | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 106 |
| Synonyms |
MENTAL RETARDATION, X-LINKED 106
MRX106
XLID106
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MENTAL RETARDATION, X-LINKED 106
MRX106
XLID106
|
|---|---|
| prefLabel | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 106
|
| Gene Symbol |
OGT
XLID106
|
| Scope Statement | Variable dysmorphic features may be present [MISCELLANEOUS]
Caused by mutation in the O-linked N-acetylglucosamine transferase gene (OGT, 300255.0001) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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|
| tui | T048
|
| Gene Locus | Xq13
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 300997
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C4478379
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |