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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