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Metadata
ID DOID:11661
Name blue color blindness
Definition A color blindness that is characterized by a selective deficiency of blue vision, has_material_basis_in autosomal dominant inheritance of a mutation in the OPN1SW gene and is associated with a deficiency or absence of blue-sensitive cone photoreceptor function.
http://www.omim.org/entry/190900, http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=88629, https://www.ncbi.nlm.nih.gov/pubmed/2788922
Xrefs

ICD10CM:H53.55

ICD9CM:368.53

MESH:D003117

OMIM:190900

SNOMEDCT_US_2023_03_01:51886007

UMLS_CUI:C0155017

Synonyms

Tritan defect [EXACT]

Tritanopia [EXACT]

Parent Relationships

is_a color blindness

is_a autosomal dominant disease

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