Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Fanconi Anemia, Complementation Group N
ID

http://purl.bioontology.org/ontology/MESH/C563657
cui

C1835817
HM

D005199
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D005199
MDA

20121105
MeSH Frequency

0
notation

C563657
prefLabel

Fanconi Anemia, Complementation Group N
SC

3
Scope Statement

mutation in PALB2
TERMUI

T803320
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_0111094 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/OMIM/610355 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/610832 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/610832 Online Mendelian Inheritance in Man LOOM