Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/615433
http://purl.bioontology.org/ontology/OMIM/615433
|
|---|---|
| Preferred Name | CHROMOSOME 3q13.31 DELETION SYNDROME |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | CHROMOSOME 3q13.31 DELETION SYNDROME
|
|---|---|
| Gene Symbol |
C13DELq13.31
DEL3q13.31
|
| Scope Statement | Contiguous gene syndrome caused by deletion (580kb-22.5Mb) of 3q13.31 [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T047
|
| Gene Locus | 3q13.31
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 615433
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C3809490
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |