A disease that has_material_basis_in genetic variations in the human genome.

This is just here as a test because I lose it

Term information

database cross reference
  • NCI:C3101
  • UMLS_CUI:C0019247
  • SNOMEDCT_US_2018_03_01:32895009
  • MESH:D030342
Subsets

NCIthesaurus

database cross reference

MESH:D030342

SNOMEDCT_US_2018_03_01:32895009

NCI:C3101

UMLS_CUI:C0019247

has obo namespace

disease_ontology

id

DOID:630

imported from

http://purl.obolibrary.org/obo/doid.owl

Term relations

Subclass of: