Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Retinitis Pigmentosa 30
ID

http://purl.bioontology.org/ontology/MESH/C564310
cui

C1842816
HM

D012174
Inverse of RB

0
Mapped to

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

20121105
MeSH Frequency

0
notation

C564310
prefLabel

Retinitis Pigmentosa 30
SC

3
Scope Statement

mutation in FSCN2
TERMUI

T804611
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/607921 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/607921 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/607643 Online Mendelian Inheritance in Man CUI
http://purl.obolibrary.org/obo/DOID_0110406 Human Disease Ontology 123 LOOM