PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
Preferred Name

Hemoglobinopathies
Synonyms
ID

http://www.phoc.org.cn/pmo/class/PMO_00036627

Database_Cross_Reference

MDR:10018902

RCDAE:X20Ci

SNOMEDCT_US:80141007

MDR:10060892

NDFRT:N0000001472

SNOMEDCT_US:267556002

NCI:C3092

SNOMEDCT_US:154794008

SNM:D-4130

SNMI:DC-20000

COSTAR:NOCODE

CSP:1418-5657

CHV:0000005994

AOD:0000005748

LCH:U002149

LNC:LP31618-9

CST:HEMRBCDIS

NCI_NICHD:C3092

LCH_NW:sh85060203

MDR:10018905

ICD10CM:D58.2

MTH:U000166

MDR:10018903

RCD:X20Ci

MSH:D006453

LNC:MTHU029621

LNC:LA16207-5

CST:HAL/RBC/HGB

MEDCIN:277675

MDR:10055610

DO:DOID:2860

CCPSS:1017538

BI:BI00313

MTHICD9:282.7

label

Hemoglobinopathies

MCID

MC00006075

PMOID

PMO:00036627

prefixIRI

pmo:PMO_00036627

prefLabel

Hemoglobinopathies

Synonym

Hemoglobinopathy NOS

HEMOGLOBINOPATHY

haemoglobinopathy

Hemoglobinopathy, NOS

diseases hemoglobin

hemoglobinopathy

Haemoglobin disease

Hemoglobinopathies [Disease/Finding]

HEMOGLOBIN DISORDER

Haemoglobin disorder

hemoglobin disorders

Hemoglobinopathy

Hemoglobin disorder

Hemoglobin disorders

hemoglobinopathies

Haemoglobinopathies

Hemoglobin disease

disorders hemoglobin

Hemoglobin disorder, NOS

Haemoglobin disease, NOS

Haemoglobinopathy, NOS

Globin abnormality

C-20 HEMOGLOBINOPATHIES

Hemoglobin disease, NOS

Haemoglobinopathy

Haemoglobinopathy NOS

hemoglobinopathy (diagnosis)

haemoglobinopathies

Haemoglobinopathies congenital

hemoglobin disease

haemoglobin disease

Hemoglobinopathies congenital

HEMOGLOBINOPATHIES

Globin abnormality, NOS

Hemoglobinopathy (disorder)

Haemoglobin disorder, NOS

hemoglobin disorder

Hemoglobinopathies / Iron Metabolism

Tree Number

T9.8.4.25

T9.5.2.2

subClassOf

http://www.phoc.org.cn/pmo/class/PMO_00036558

http://www.phoc.org.cn/pmo/class/PMO_00037325

Delete Subject Author Type Created
No notes to display