Split-Foot Malformation with Mesoaxial Polydactyly (SFMMP)

Alias:
Split-Foot Malformation-Mesoaxial Polydactyly Syndrome
Sfmmp
Split-Foot Malformation-Mesoaxial Polydactyly-Nail Abnormalities-Sensorineural Hearing Loss Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Split-Foot Malformation with Mesoaxial Polydactyly, also known as split-foot malformation-mesoaxial polydactyly syndrome, is related to split-hand/foot malformation 1. An important gene associated with Split-Foot Malformation with Mesoaxial Polydactyly is MAP3K20 (Mitogen-Activated Protein Kinase Kinase Kinase 20). Affiliated tissues include skin and bone, and related phenotypes are split foot and bilateral sensorineural hearing impairment
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
1
7
2

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
No Data Found!
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