Disease #01979 (OODD (dysplasia, odontoonychodermal (OODD)), OMIM:257980)
Official abbreviation |
OODD |
Name |
dysplasia, odontoonychodermal (OODD) |
OMIM ID |
257980 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
WNT10A |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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