Disease #00666 (MOTA (Manitoba oculotrichoanal syndrome (MOTA)), OMIM:248450)
Official abbreviation |
MOTA |
Name |
Manitoba oculotrichoanal syndrome (MOTA) |
OMIM ID |
248450 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
FREM1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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