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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/609625
http://purl.bioontology.org/ontology/OMIM/609625
|
|---|---|
| Preferred Name | CHROMOSOME 10q26 DELETION SYNDROME |
| Synonyms |
TERMINAL CHROMOSOME 10q26 DELETION SYNDROME
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | TERMINAL CHROMOSOME 10q26 DELETION SYNDROME
|
|---|---|
| prefLabel | CHROMOSOME 10q26 DELETION SYNDROME
|
| Gene Symbol |
C10q26DEL
DEL10q26
|
| Scope Statement | Caused by deletion of at least 600kb in 10q26.2 [MOLECULAR BASIS]
Contiguous gene deletion syndrome [MISCELLANEOUS]
Highly variable phenotype [MISCELLANEOUS]
Cases reported include de novo deletions, interstitial deletions, and translocations involving only the terminal band of the reciprocal chromosome [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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| tui | T047
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| Gene Locus | 10q26
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| MIMTYPEMEANING | Phenotype description, molecular basis known.
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| notation | 609625
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| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C2674937
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| OMIM Entry Type | 3
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| OMIM MimType Value | pound
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| Delete | Subject | Author | Type | Created |
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| No notes to display |