Disease #05815 (CPSFS1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome, type 1B), OMIM:618469)
Official abbreviation |
CPSFS1B |
Name |
contractures, pterygia, and spondylocarpotarsal fusion syndrome, type 1B |
OMIM ID |
618469 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
MYH3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2020-08-24 09:56:53 +02:00 (CEST) |
Date last edited |
2021-12-10 23:14:50 +01:00 (CET) |
Individuals
|