PMO Precision Medicine Ontology - Congenital Hemolytic Anemia - Classes | NCBO BioPortal

PMO Precision Medicine Ontology

Last uploaded: December 16, 2020

Id	http://www.phoc.org.cn/pmo/class/PMO_00000971 http://www.phoc.org.cn/pmo/class/PMO_00000971
Preferred Name	Congenital Hemolytic Anemia
Definitions	A form of hemolytic anemia with congenital onset.
Type	http://www.w3.org/2002/07/owl#Class

label	Congenital Hemolytic Anemia
prefLabel	Congenital Hemolytic Anemia
Synonym	Anemia, Hemolytic, Congenital [Disease/Finding] CONGEN HEMOLYTIC ANEMIA Congenital haemolytic anaemia, NOS Hereditary haemolytic anaemia NOS Anemias, Hereditary Hemolytic Hereditary hemolytic anemia (disorder) Congenital haemolytic anemia HEMOLYTIC ANEMIA CONGEN Congenital hemolytic anemia NOS Hereditary haemol. anemia NOS anaemias haemolytics hereditary Hereditary hemolytic anemia, NOS Anemia, Hemolytic, Hereditary Hereditary hemolytic anemia NOS Congenital haemolytic anaemia NOS Hereditary haemolytic anaemia, NOS Hereditary haemol.anaem Hemolytic Anemia, Congenital Hemolytic Anemias, Congenital Other hered. hem. anemias Hemolytic Anemia, Hereditary Hemolytic Anemias, Hereditary Hereditary haemolytic anaemia, unspecified Hereditary haemol. anaemia NOS Hereditary hemolytic anemia NOS (disorder) hereditary haemolytic anaemias Anemia, Hereditary Hemolytic Congenital hemolytic anemia, NOS Anemia -heredit.hemol Hereditary Hemolytic Anemias Congenital Hemolytic Anemias Anemia;hemolytic;hereditary Hereditary haemolytic anaemia Congenital haemolytic anaemia Hered hemolytic anem NOS Anemias, Congenital Hemolytic ANEMIA HEMOLYTIC CONGEN Hereditary hemolytic anemia congenital hemolytic anemia Anemia, Congenital Hemolytic Hereditary hemol.anaem ANEMIA HEMOLYTIC HEREDITARY Anemia, Hemolytic, Congenital Congenital hemolytic anemia (disorder) Anaemia;haemolytic;hereditary hereditary hemolytic anemia (diagnosis) Hereditary hemolytic anemia, unspecified Other hered. haem. anaemias Anaemia -heredit.haemol See more See less
Definition	A form of hemolytic anemia with congenital onset.
PMOID	PMO:00000971
MCID	MC00000886
prefixIRI	pmo:PMO_00000971
Database_Cross_Reference	SNOMEDCT_US:267558001 RCD:D10.. CCPSS:0007106 MDR:10019886 SNOMEDCT_US:267556002 ICD10AMAE:D58.9 SNOMEDCT_US:154794008 SNMI:DC-10108 OMIM:MTHU052589 ICD10:D58.9 ICPC2EENG:B78 MDR:10019880 ICD9CM:282.9 MDR:10019881 ICPC2P:B78003 SNMI:DC-10107 MSH:D000745 ICD9CM:282 MTHICD9:282.0 SNOMEDCT_US:154801000 ICD10AM:D58.9 MDR:10054399 MEDCIN:97962 MDR:10055202 MDR:10010489 NCI:C34379 MDR:10073793 MDR:10019885 MTHICD9:282.9 HPO:HP:0004804 AOD:0000005946 CHV:0000001126 ICD10CM:D58.9 MDR:10060893 SNOMEDCT_US:42601008 RCDAE:D10.. SNOMEDCT_US:191208008 RCDAE:D10z. NDFRT:N0000000389 DO:DOID:589 CSP:0427-1351 RCD:D10z. MDR:10019882 SNOMEDCT_US:38911009 See more See less
Tree Number	T3.2.2.8.2.2.3
subClassOf	http://www.phoc.org.cn/pmo/class/PMO_00036558 http://www.phoc.org.cn/pmo/class/PMO_00037326 http://www.phoc.org.cn/pmo/class/PMO_00000966
equivalentClass	http://www.phoc.org.cn/pmo/class/PMO_00036561
type	http://www.w3.org/2002/07/owl#Class

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