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's subclass of is recorded as short rib – polydactyly syndrome^[4].
• Verma-Naumoff syndrome's subclass of is recorded as asphyxiating thoracic dysplasia^[5].
• Verma-Naumoff syndrome's subclass of is recorded as autosomal recessive disease^[6].
• Verma-Naumoff syndrome's OMIM ID is recorded as 613091^[7].
• Verma-Naumoff syndrome's ICD-10 ID is recorded as Q77.2^[8].
• Verma-Naumoff syndrome's Disease Ontology ID is recorded as DOID:0110087^[9].
• Verma-Naumoff syndrome's Orphanet ID is recorded as 93271^[10].
• Verma-Naumoff syndrome's NCI Thesaurus ID is recorded as C163755^[11].
• Verma-Naumoff syndrome's health specialty is recorded as medical genetics^[12].
• Verma-Naumoff syndrome's genetic association is recorded as DYNC2H1^[13].
• Verma-Naumoff syndrome's genetic association is recorded as WDR35^[14].
• Verma-Naumoff syndrome's genetic association is recorded as DYNC2I2^[15].
• Verma-Naumoff syndrome's genetic association is recorded as DYNC2I1^[16].
• Verma-Naumoff syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110087^[17].
• Verma-Naumoff syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0110087^[18].
• Verma-Naumoff syndrome's UMLS CUI is recorded as C0432197^[19].
• Verma-Naumoff syndrome's Medical Dictionary for Regulatory Activities ID is recorded as 10048893^[20].
• Verma-Naumoff syndrome's ICD-10-CM is recorded as Q77.2^[21].
• Verma-Naumoff syndrome's GARD rare disease ID is recorded as 4835^[22].
• Verma-Naumoff syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[23].
• Verma-Naumoff syndrome's Mondo ID is recorded as MONDO_0013127^[24].
• Verma-Naumoff syndrome's UniProt disease ID is recorded as DI-02583^[25].