General Information of Disease (ID: DISNSX3G)

Disease Name Autosomal genetic disease
Synonyms autosomal inherited disorder; autosomal inherited disease; autosomal hereditary disorder
Definition A monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes.
Disease Hierarchy
DISYKSRF: Genetic disease
DISNSX3G: Autosomal genetic disease
Disease Identifiers
MONDO ID
MONDO_0000429
UMLS CUI
C0265384
MedGen ID
539205
SNOMED CT ID
1899006