Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

FANCONI ANEMIA, COMPLEMENTATION GROUP N
Synonyms

FANCN
ID

http://purl.bioontology.org/ontology/OMIM/610832
altLabel

FANCN
cui

C1835817
Gene Locus

16p12
Gene Symbol

PNCA3

FANCN

PALB2
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

610832
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

FANCONI ANEMIA, COMPLEMENTATION GROUP N
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/MESH/C563657 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C563657 Medical Subject Headings LOOM