Experimental Factor Ontology

Last uploaded: December 16, 2024
Preferred Name

megaloblastic anemia
Synonyms

IGS

recessive hereditary megaloblastic anaemia 1

MGA1 Norwegian type

megaloblastic anemia

megaloblastic anemia (disease)

Grasbeck-Imerslund syndrome

recessive hereditary megaloblastic anemia 1

megaloblastic anaemia (disease)

RH-MGA1

Definitions

Anemia characterized by the presence of unusually large erythroblasts in the bone marrow called megaloblasts. It is usually caused by vitamin B12 or folic acid deficiency. Other causes include toxins and drugs.

ID

http://purl.obolibrary.org/obo/MONDO_0001700

database_cross_reference

MEDGEN:1527

NANDO:2100176

UMLS:C0002888

SCTID:53165003

NANDO:2200612

NCIT:C34382

DOID:13382

HP:0001889

ICD9:281.3

definition

Anemia characterized by the presence of unusually large erythroblasts in the bone marrow called megaloblasts. It is usually caused by vitamin B12 or folic acid deficiency. Other causes include toxins and drugs.

exactMatch

http://identifiers.org/medgen/1527

http://purl.obolibrary.org/obo/NCIT_C34382

http://identifiers.org/snomedct/53165003

http://purl.obolibrary.org/obo/DOID_13382

http://linkedlifedata.com/resource/umls/id/C0002888

has_exact_synonym

recessive hereditary megaloblastic anaemia 1

MGA1 Norwegian type

megaloblastic anemia

megaloblastic anemia (disease)

Grasbeck-Imerslund syndrome

recessive hereditary megaloblastic anemia 1

megaloblastic anaemia (disease)

RH-MGA1

has_related_synonym

IGS

IAO_0000589

megaloblastic anemia (disease)

id

MONDO:0001700

in_subset

http://purl.obolibrary.org/obo/mondo#rare

http://purl.obolibrary.org/obo/mondo#otar

http://purl.obolibrary.org/obo/mondo#gard_rare

label

megaloblastic anemia

notation

MONDO:0001700

preferred label

megaloblastic anemia

prefLabel

megaloblastic anemia

subClassOf

http://purl.obolibrary.org/obo/MONDO_0002281

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Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0001700 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0001700 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0001700 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0001700 KTAO SAME_URI
http://purl.obolibrary.org/obo/DOID_13382 DOID LOOM
http://pat.nichd.nih.gov/maternalconditions/C0002888 PATMHC LOOM
http://purl.jp/bio/4/id/200906082001576472 IOBC LOOM
http://www.limics.org/hrdo/rdfns#sgn_id_48280 HRDO LOOM
http://purl.obolibrary.org/obo/NCIT_C34382 BERO LOOM
http://nanbyodata.jp/ontology/NANDO_2100176 NANDO LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2329 IFAR LOOM
http://purl.obolibrary.org/obo/MONDO_0001700 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0001700 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0001700 DOVES LOOM
http://purl.obolibrary.org/obo/DOID_13382 BAO LOOM
http://purl.obolibrary.org/obo/DOID_13382 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_13382 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_13382 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_13382 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_13382 FNS-H LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/53165003 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/MEDDRA/10027129 MEDDRA LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0002888 OCHV LOOM
http://www.phoc.org.cn/pmo/class/PMO_00000993 PMAPP-PMO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34382 NCIT LOOM
http://nanbyodata.jp/ontology/NANDO_2200612 NANDO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_13382 NATPRO LOOM
http://localhost/plosthes.2017-1#6318 PLOSTHES LOOM
http://purl.obolibrary.org/obo/HP_0001889 CCONT LOOM
http://purl.obolibrary.org/obo/HP_0001889 SCDO LOOM
http://purl.obolibrary.org/obo/HP_0001889 HP LOOM
http://purl.obolibrary.org/obo/HP_0001889 UPHENO LOOM
http://purl.bioontology.org/ontology/CST/ANEMIA%20MEGALOBLAST COSTART LOOM
rgo:34496 GAMUTS LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Megaloblastic_Anemia CSEO LOOM
http://purl.bioontology.org/ontology/CSP/0427-2735 CRISP LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU008399 OMIM LOOM