Disease #00699 (dysplasia, Czech, OMIM:609162)
Official abbreviation |
- |
Name |
dysplasia, Czech |
OMIM ID |
609162 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
5 |
Phenotype entries for this disease |
4 |
Associated with 1 gene |
COL2A1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|