Disease #02985 (HPE7 (holoprosencephaly, type 7 (HPE-7)), OMIM:610828)
Official abbreviation |
HPE7 |
Name |
holoprosencephaly, type 7 (HPE-7) |
OMIM ID |
610828 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
7 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
PTCH1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|