Log In|Sign Up
ENSplit-Hand/foot Malformation 6 (SHFM6)
Alias:
Split Hand-Foot Malformation 6
Shfm6
Split-Hand/foot Malformation, Type 6
Ectrodactyly, Autosomal Recessive
Ectrodactyly Autosomal Recessive
Favorite
Split-Hand/foot Malformation 6, also known as split hand-foot malformation 6, is related to split hand-foot malformation and orofacial cleft 4. An important gene associated with Split-Hand/foot Malformation 6 is WNT10B (Wnt Family Member 10B), and among its related pathways/superpathways are MECP2 and associated Rett syndrome and Validated transcriptional targets of deltaNp63 isoforms. Affiliated tissues include bone, and related phenotypes are split hand and finger syndactyly
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
