Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Usher Syndrome, Type IF
ID

http://purl.bioontology.org/ontology/MESH/C566586
cui

C1865885
HM

D052245
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D052245
MDA

20120824
MeSH Frequency

0
notation

C566586
prefLabel

Usher Syndrome, Type IF
SC

3
Scope Statement

aka USH1F; associated with mutation in PCDH15
TERMUI

T827949
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/602083 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/602083 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/605514 Online Mendelian Inheritance in Man CUI