Disease #01704 (KFS2 (Klippel-Feil syndrome, type 2, autosomal recessive (KFS-2)), OMIM:214300)
Official abbreviation |
KFS2 |
Name |
Klippel-Feil syndrome, type 2, autosomal recessive (KFS-2) |
OMIM ID |
214300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
MEOX1 |
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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|