Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Newfoundland Rod-Cone Dystrophy
ID

http://purl.bioontology.org/ontology/MESH/C564391
cui

C1843815
HM

D012174
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D012174
MDA

20121105
MeSH Frequency

1
notation

C564391
prefLabel

Newfoundland Rod-Cone Dystrophy
SC

3
Scope Statement

RLBP1 protein, human mutation
TERMUI

T804791
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/180090 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/607476 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/607476 Online Mendelian Inheritance in Man LOOM