Verma-Naumoff syndrome
Human disease
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Verma-Naumoff syndrome
Summary
Verma-Naumoff syndrome is a hereditary disorder[1].
Key Facts
- Verma-Naumoff syndrome's instance of is recorded as hereditary disorder[2].
- Verma-Naumoff syndrome's instance of is recorded as class of disease[3].
- Verma-Naumoff syndrome is a type of short rib – polydactyly syndrome[4].
- Verma-Naumoff syndrome is a type of asphyxiating thoracic dysplasia[5].
- Verma-Naumoff syndrome is a type of autosomal recessive disease[6].
- Verma-Naumoff syndrome's NCI Thesaurus ID is recorded as C163755[7].
- Verma-Naumoff syndrome's health specialty is recorded as medical genetics[8].
- Verma-Naumoff syndrome's genetic association is recorded as DYNC2H1[9].
- Verma-Naumoff syndrome's genetic association is recorded as WDR35[10].
- Verma-Naumoff syndrome's genetic association is recorded as DYNC2I2[11].
- Verma-Naumoff syndrome's genetic association is recorded as DYNC2I1[12].
- Verma-Naumoff syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110087[13].
- Verma-Naumoff syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0110087[14].
- Verma-Naumoff syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].