Hemoglobin M [hemoglobin M]
A group of abnormal hemoglobins in which amino acid substitutions take place in either the alpha or beta chains but near the heme iron. This results in facilitated oxidation of the hemoglobin to yield excess methemoglobin which leads to cyanosis.
- Annotation
- /urine: coordinate with HEMOGLOBINURIA
- DUI
- D006449 MeSH Browser
- CUI
- M0010123
- CAS
- Hemoglobin M
- Previous indexing
- Hemoglobins, Abnormal (1966-1976)
- History note
- 91(77); was see under HEMOGLOBINS, ABNORMAL 1977-90
- Public note
- 91; was see under HEMOGLOBINS, ABNORMAL 1977-90
Allowable subheadings
- AD
- administration & dosage
- AE
- adverse effects
- AG
- agonists
- AA
- analogs & derivatives
- AN
- analysis
- AI
- antagonists & inhibitors
- BI
- biosynthesis
- CF
- cerebrospinal fluid
- CS
- chemical synthesis
- CH
- chemistry
- CL
- classification
- DF
- deficiency
- DE
- drug effects
- EC
- economics
- GE
- genetics
- HI
- history
- IM
- immunology
- IP
- isolation & purification 1
- ME
- metabolism
- PK
- pharmacokinetics
- PD
- pharmacology
- PH
- physiology 1
- PO
- poisoning
- RE
- radiation effects
- ST
- standards
- SD
- supply & distribution
- TU
- therapeutic use
- TO
- toxicity 1
- UL
- ultrastructure
- UR
- urine
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