Disease #04421 (UCMD2 (dystrophy, muscular, congenital, Ullrich, type 2?, (UCMD-2)), OMIM:616470)
Official abbreviation |
UCMD2 |
Name |
dystrophy, muscular, congenital, Ullrich, type 2?, (UCMD-2) |
OMIM ID |
616470 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
COL12A1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|