Search Ontology:
Human Disease

achromatopsia

Term ID
DOID:13911
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_2023_03_01:56852002
  • UMLS_CUI:C0152200
Ontology
Human Disease   ( DOID:13911 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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