Human Disease and Mouse Model Detail
|
Human Disease
|
Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly
OMIM ID: 228930
|
|
Synonyms
|
Fuhrmann Syndrome
|
|
View all models
|
View ALL (2) mouse models for this human disease.
|
Genes and
mouse models
|
Mutations in human and/or mouse homologs are associated with this disease
| |
|
|
*Gene is associated with the disease in this species |
| |
|
|
  | | |
Wnt7a*
|
WNT7A*
|
View 2 models
|
1:1 Homology
|
|
Mouse Models
Human Disease Modeled: Fibular Aplasia or Hypoplasia, Femoral Bowing and Poly-, Syn-, and Oligodactyly
Associated Mouse Gene:
Wnt7a
Analysis Tools