Disease #01460 (NFJS (Naegeli-Franceschetti-Jadassohn syndrome), OMIM:161000)
Official abbreviation |
NFJS |
Name |
Naegeli-Franceschetti-Jadassohn syndrome |
OMIM ID |
161000 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
KRT14 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|