Link to this page
Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/603902
http://purl.bioontology.org/ontology/OMIM/603902
|
|---|---|
| Preferred Name | BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE |
| Synonyms |
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, IRISH OR WEATHERALL TYPE
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | DYSERYTHROPOIETIC ANEMIA, CONGENITAL, IRISH OR WEATHERALL TYPE
|
|---|---|
| prefLabel | BETA-THALASSEMIA, DOMINANT INCLUSION BODY TYPE
|
| Gene Symbol |
ECYT6
HBB
|
| Scope Statement | Caused by mutation in the hemoglobin beta gene (HBB, 141900.0314) [MOLECULAR BASIS]
|
| type | |
| Has manifestation |
See more
See less
|
| tui | T047
|
| Gene Locus | 11p15.5
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 603902
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1858990
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |