Disease #01544 (RB1 (retinoblastoma, type 1), OMIM:180200)
Official abbreviation |
RB1 |
Name |
retinoblastoma, type 1 |
OMIM ID |
180200 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant, Somatic mutation |
Individuals reported having this disease |
67 |
Phenotype entries for this disease |
66 |
Associated with 1 gene |
RB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2025-01-14 18:01:23 +01:00 (CET) |
Individuals
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