Disease #07091 (LADD2 (lacrimoauriculodentodigital syndrome, type 2), OMIM:620192)
| Official abbreviation |
LADD2 |
| Name |
lacrimoauriculodentodigital syndrome, type 2 |
| OMIM ID |
620192 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FGFR3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-05-31 10:16:12 +02:00 (CEST) |
| Date last edited |
N/A |
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