OBO ID: DOID:13911
Term Name: achromatopsia Search Ontology:
Synonyms:
  • ACHM
  • Monochromatism
Definition: A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. (4)
References:
  • ICD10CM:H53.51
  • ICD9CM:368.54
  • MESH:D003117
  • NCI:C84528
  • ORDO:49382
  • SNOMEDCT_US_2020_09_01:56852002
  • UMLS_CUI:C0152200
Ontology: Human Disease   (DOID:13911)
OTHER achromatopsia PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS
Fish Conditions Citations
gnat2w21/w21(AB) standard conditions Kennedy et al., 2007
PHENOTYPE No data available

CITATIONS (2)