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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/300433
http://purl.bioontology.org/ontology/OMIM/300433
|
|---|---|
| Preferred Name | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 81 |
| Synonyms |
XLID81
MENTAL RETARDATION, X-LINKED 81
MRX81
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
XLID81
MENTAL RETARDATION, X-LINKED 81
MRX81
|
|---|---|
| prefLabel | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 81
|
| Gene Symbol |
MRX81
XLID81
|
| Scope Statement | Obligate carrier females have normal intelligence [MISCELLANEOUS]
No consistent features other than mental retardation [MISCELLANEOUS]
Based on a report of 9 affected males from one Italian family [MISCELLANEOUS]
|
| type | |
| Has manifestation | |
| tui | T048
|
| Gene Locus | Xp11.2-q12
|
| MIMTYPEMEANING | Mendelian phenotype or locus, molecular basis unknown.
|
| notation | 300433
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1845531
|
| OMIM Entry Type | 5
|
| OMIM MimType Value | perc
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |