Medical Subject Headings

Last uploaded: January 31, 2024

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Preferred Name	Elliptocytosis, Hereditary
Synonyms	Elliptocytoses, Hereditary
Definitions	An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
ID	http://purl.bioontology.org/ontology/MESH/D004612
altLabel	Elliptocytoses, Hereditary Hereditary Elliptocytosis Ovalocytoses, Hereditary Ovalocytosis, Hereditary Hereditary Ovalocytosis Hereditary Elliptocytoses Hereditary Ovalocytoses
AN	a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
AQL	BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
cui	C0013902
DC	1
definition	An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
DX	19650101
FX	D000756
HN	65(64)
Inverse of AQ	http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000401
Inverse of RO	http://purl.bioontology.org/ontology/MESH/D000756
Machine permutation	65
Mapped from	http://purl.bioontology.org/ontology/MESH/C563479 http://purl.bioontology.org/ontology/MESH/C564570 http://purl.bioontology.org/ontology/MESH/C566678 http://purl.bioontology.org/ontology/MESH/C565598 http://purl.bioontology.org/ontology/MESH/C566231 http://purl.bioontology.org/ontology/MESH/C565058 http://purl.bioontology.org/ontology/MESH/C564215 http://purl.bioontology.org/ontology/MESH/C563004 http://purl.bioontology.org/ontology/MESH/C567520 http://purl.bioontology.org/ontology/MESH/C563480
MDA	19990101
MMR	20230226
MN	C16.320.070.365 C15.378.050.141.150.365
notation	D004612
prefLabel	Elliptocytosis, Hereditary
TERMUI	T014076 T014077
TH	UNK (19XX) NLM (1964)
tui	T047
subClassOf	http://purl.bioontology.org/ontology/MESH/D000745

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10019877	MDRGER	CUI
http://purl.bioontology.org/ontology/MDRGER/10014490	MDRGER	CUI
http://purl.bioontology.org/ontology/CSP/0427-1524	CRISP	CUI
http://purl.bioontology.org/ontology/MSHFRE/D004612	MSHFRE	CUI
http://purl.bioontology.org/ontology/ICD9CM/282.1	ICD9CM	CUI
http://purl.bioontology.org/ontology/SNMI/DC-15300	SNMI	CUI
http://purl.bioontology.org/ontology/RCD/D101.	RCD	CUI
http://purl.bioontology.org/ontology/MEDDRA/10019877	MEDDRA	CUI
http://purl.bioontology.org/ontology/NDFRT/N0000001064	NDFRT	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/191169008	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/ICD10/D58.1	ICD10	CUI
http://purl.bioontology.org/ontology/MDRFRE/10014490	MDRFRE	CUI
http://purl.bioontology.org/ontology/MDRFRE/10019877	MDRFRE	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU027001	OMIM	CUI
http://purl.bioontology.org/ontology/ICD10CM/D58.1	ICD10CM	CUI
http://purl.bioontology.org/ontology/MEDDRA/10014490	MEDDRA	CUI
http://purl.bioontology.org/ontology/SCTSPA/191169008	SCTSPA	CUI
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.070.365	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C15.378.071.141.150.365	RH-MESH	LOOM
http://purl.jp/bio/4/id/200906087883343969	IOBC	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036564	PMAPP-PMO	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D004612	RH-MESH	LOOM
http://id.nlm.nih.gov/mesh/D004612	MDM	LOOM
http://purl.obolibrary.org/obo/OMIT_0005860	OMIT	LOOM
http://purl.bioontology.org/ontology/MEDDRA/10014490	MEDDRA	LOOM