Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Jump to:
Spinner 000000 16px loading...
Preferred Name

Color vision defects
ID

http://purl.bioontology.org/ontology/OMIM/MTHU006100
cui

C0009398
Manifestation of

http://purl.bioontology.org/ontology/OMIM/615973

http://purl.bioontology.org/ontology/OMIM/601152
notation

MTHU006100
prefLabel

Color vision defects
tui

T047
subClassOf

http://purl.bioontology.org/ontology/OMIM/MTHU000020
Add comment
Add proposal
Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/ICD10CM/H53.5 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D003117 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D003117 Medical Subject Headings LOOM
http://purl.bioontology.org/ontology/ICD10/H53.5 International Classification of Diseases, Version 10 CUI