Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Retinitis Pigmentosa 41
Synonyms

Retinal Degeneration, Autosomal Recessive, Prominin-Related
ID

http://purl.bioontology.org/ontology/MESH/C567422
altLabel

Retinal Degeneration, Autosomal Recessive, Prominin-Related
cui

C2677516
HM

D012174
Inverse of RB

0
Mapped to

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

20121105
MeSH Frequency

0
notation

C567422
prefLabel

Retinitis Pigmentosa 41
SC

3
Scope Statement

mutations in PROM1; aka RP41
TERMUI

T810384

T810382
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0110376 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/604365 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/612095 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/612095 Online Mendelian Inheritance in Man LOOM