Disease #01709 (RCDP-1 (chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1)), OMIM:215100)
Official abbreviation |
RCDP-1 |
Name |
chondrodysplasia punctata, rhizomelic, type 1 (RCDP-1) |
OMIM ID |
215100 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
PEX7 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|