Forney robinson pascoe syndrome
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Forney robinson pascoe syndrome
Summary
Forney robinson pascoe syndrome is a hereditary disorder[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- Forney robinson pascoe syndrome's instance of is recorded as hereditary disorder[3].
- Forney robinson pascoe syndrome's instance of is recorded as head and neck disease[4].
- Forney robinson pascoe syndrome's instance of is recorded as developmental defect during embryogenesis[5].
- Forney robinson pascoe syndrome's instance of is recorded as rare disease[6].
- Forney robinson pascoe syndrome's instance of is recorded as class of disease[7].
- Forney robinson pascoe syndrome is a type of syndromic genetic deafness[8].
- Forney robinson pascoe syndrome is a type of genetic disease[9].
- Forney robinson pascoe syndrome's genetic association is recorded as MAP3K7[10].
- Forney robinson pascoe syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3238[11].
Why It Matters
Forney robinson pascoe syndrome is known by 10 alternative names across languages and contexts.[2]