Disease #05829 (RCDP5 (chondrodysplasia punctata, rhizomelic, type 5 (RCDP5)), OMIM:616716)
Official abbreviation |
RCDP5 |
Name |
chondrodysplasia punctata, rhizomelic, type 5 (RCDP5) |
OMIM ID |
616716 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
AR |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PEX5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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