FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term achromatopsia ID (Ontology) DOID:13911 (Human Disease)
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.
Also Known As "ACHM" ; "Monochromatism"
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  blindness
   |__color blindness
       |__achromatopsia  4 rec.
           |__achromatopsia 2 1 rec.
           |__achromatopsia 3 1 rec.
           |__achromatopsia 4 1 rec.
           |__achromatopsia 7 1 rec.
           |__blue cone monochromacy
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Is a color blindness
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Synonyms
  • "ACHM" EXACT OMO:0003012
    "Monochromatism" EXACT
Secondary IDs
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ICD10CM:H53.51
ICD9CM:368.54
MESH:D003117
NCI:C84528
ORDO:49382
SNOMEDCT_US_2023_03_01:56852002
UMLS_CUI:C0152200