Preferred Label : Hemoglobin, high altitude adaptation;
Symbol : HALAH;
CISMeF acronym : HALAH;
Type : Phenotype, molecular basis known;
Alternative titles and symbols : Hemoglobin, high oxygen saturation of;
Inheritance : Autosomal dominant;
Molecular basis : Caused by mutation in the egl-9 family hypoxia inducible factor 1 gene (EGLN1, 606425.0004);
Prefixed ID : #609070;
Origin ID : 609070;
UMLS CUI : C1836778;
Genes related to phenotype
- Semantic type(s)
