Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Night Blindness, Congenital Stationary, Autosomal Dominant 1
Synonyms

Night Blindness, Congenital Stationary, Rhodopsin-Related
ID

http://purl.bioontology.org/ontology/MESH/C566474
altLabel

Night Blindness, Congenital Stationary, Rhodopsin-Related

CSNBAD1
cui

C1864869
HM

D015785

D009755
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D015785

http://purl.bioontology.org/ontology/MESH/D009755
MDA

20121105
MeSH Frequency

0
notation

C566474
prefLabel

Night Blindness, Congenital Stationary, Autosomal Dominant 1
SC

3
Scope Statement

mutation in rhodopsin
TERMUI

T824420

T808577

T808576
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/180380 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/610445 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/610445 Online Mendelian Inheritance in Man LOOM