Disease #01000 (DA7 (Trismus-pseudocamptodactyly syndrome), OMIM:158300)
Official abbreviation |
DA7 |
Name |
Trismus-pseudocamptodactyly syndrome |
OMIM ID |
158300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
MYH8 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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