Split-foot Malformation-mesoaxial Polydactyly Syndrome
Table of contents:
Genes related to Split-foot Malformation-mesoaxial Polydactyly Syndrome
- MAP3K20
Clinical Features
Phenotypes and symptoms related to Split-foot Malformation-mesoaxial Polydactyly Syndrome
- Hearing impairment
- Sensorineural hearing impairment
- Syndactyly
- Polydactyly
- Bilateral sensorineural hearing impairment
- Cutaneous syndactyly
- Split foot
- Mesoaxial polydactyly
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Alternative names
Split-foot Malformation-mesoaxial Polydactyly Syndrome Is also known as split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome, sfmmp.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Split-foot Malformation-mesoaxial Polydactyly Syndrome Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 ZAK.
By Fulgent Genetics Fulgent Genetics (United States).
MAP3K20
Specificity
100 %
Genes
100 % |
You can get up to -7 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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