Preferred Name |
Hemoglobin M Disease |
ID |
http://purl.bioontology.org/ontology/MESH/C581942 |
cui |
C3665425 |
Has mapping qualifier | |
HM |
D006449 D008708/Q000151 |
Inverse of RB |
0 |
Mapped to | |
MDA |
20131106 |
MeSH Frequency |
4 |
notation |
C581942 |
prefLabel |
Hemoglobin M Disease |
SC |
3 |
Scope Statement |
promote; specific types of Hemoglobin M disease (methemoglobinemia due to hemoglobin M beta types, or alpha types) represented by several scr |
TERMUI |
T842000 |
TH |
GHR (2014) |
tui |
T047 |
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/ICD10CM/D74.0 | International Classification of Diseases, Version 10 - Clinical Modification | CUI |