Disease #03396 (KFS3 (Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3)), OMIM:613702)
| Official abbreviation |
KFS3 |
| Name |
Klippel-Feil syndrome, type 3, autosomal dominant (KFS-3) |
| OMIM ID |
613702 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
GDF3 |
| 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
|