Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

UNC119, C. ELEGANS, HOMOLOG OF
Synonyms

UNC119
ID

http://purl.bioontology.org/ontology/OMIM/604011
altLabel

UNC119

HUMAN RETINAL GENE 4

IMMUNODEFICIENCY 13 (1 family)

CONE-ROD DYSTROPHY

HRG4
cui

C1421355

C0035334

C4016870
Gene Locus

17q11.2
Gene Symbol

UNC119

IMD13

HRG4
Has allelic variant

http://purl.bioontology.org/ontology/OMIM/604011.0002

http://purl.bioontology.org/ontology/OMIM/604011.0001
MIMTYPEMEANING

Gene with known sequence and phenotype
notation

604011
OMIM Entry Type

4
OMIM MimType Value

plus
prefLabel

UNC119, C. ELEGANS, HOMOLOG OF
tui

T028

T033

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/D012174 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/H35.52 International Classification of Diseases, Version 10 - Clinical Modification CUI