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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/301024
http://purl.bioontology.org/ontology/OMIM/301024
|
|---|---|
| Preferred Name | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108 |
| Synonyms |
MENTAL RETARDATION, X-LINKED 108
MRX108
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
MENTAL RETARDATION, X-LINKED 108
MRX108
|
|---|---|
| prefLabel | INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108
|
| Gene Symbol |
NHE7
SLC9A7
MRX108
|
| Scope Statement | Two unrelated families have been reported (last curated April 2019) [MISCELLANEOUS]
Caused by mutation in the solute carrier family 9, member 7 gene (SLC9A7, 300368.0001) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | Xp11.3
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 301024
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C5193009
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
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| No notes to display |