Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Macular Dystrophy, Retinal, 2
ID

http://purl.bioontology.org/ontology/MESH/C562746
cui

C0339512
HM

D003317
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D003317
MDA

20121105
MeSH Frequency

1
notation

C562746
prefLabel

Macular Dystrophy, Retinal, 2
SC

3
Scope Statement

mutation in PROM1
TERMUI

T801414
TH

OMIM (2013)
tui

T019
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/604365 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/608051 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/608051 Online Mendelian Inheritance in Man LOOM