Disease #00115 (HPE7 (HOLOPROSENCEPHALY 7), OMIM:610828)
Official abbreviation |
HPE7 |
Name |
HOLOPROSENCEPHALY 7 |
OMIM ID |
610828 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PTCH1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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