Disease #05101 (adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome), OMIM:129200)
| Official abbreviation |
- |
| Name |
adermatoglyphia, congenital facial milia, acral blisters, digital contractures, nail abnormalities (Basan syndrome) |
| OMIM ID |
129200 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-11-10 10:55:30 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|