Disease #00967 (Bowen-Conradi syndrome, OMIM:211180)
Official abbreviation |
- |
Name |
Bowen-Conradi syndrome |
OMIM ID |
211180 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
EMG1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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