MeSH Browser

MeSH Supplementary: hemoglobin F Meinohama
Unique ID: C033429
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C033429
Entry Term(s): HBGG g.17A>G; Hb F Meinohama; Hb F-Meinohama; hemoglobin F-Meinohama
Registry Numbers: 81031-42-7
Heading Mapped to: *Fetal Hemoglobin; *Hemoglobins, Abnormal
Frequency: 1
Note: fetal Hb variant; Gly replaced by Gln at position 5(A2) on gamma chain; abnormal gamma chain has Ile at position 75 & Gly at position 136
Source: Hemoglobin 1981;5(6):565
Date of Entry: 1982/02/22
Revision Date: 2004/11/05

Concept UI: M0103690
Registry Numbers: 81031-42-7
Terms: hemoglobin F Meinohama Preferred Term
Term UI T133694
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1982); Hb F Meinohama
Term UI T133691
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1982); Hb F-Meinohama
Term UI T133692
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1982); HBGG g.17A>G
Term UI T590357
Date06/10/2004
LexicalTag NON
ThesaurusID NLM (2004); hemoglobin F-Meinohama
Term UI T133693
Date01/01/1955
LexicalTag NON
ThesaurusID NLM (1982)

hemoglobin F Meinohama MeSH Supplementary Concept Data 2025