Disease #01768 (SHFM6 (split-hand/foot malformation, type 6 (SHFM-6)), OMIM:225300)
Official abbreviation |
SHFM6 |
Name |
split-hand/foot malformation, type 6 (SHFM-6) |
OMIM ID |
225300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
6 |
Associated with 1 gene |
WNT10B |
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
|