Preferred Label : Alopecia, androgenetic, 1;
Symbol : AGA1;
CISMeF acronym : AGA; AGA1; MPB;
Type : Phenotype or locus, molecular basis unknown;
Alternative titles and symbols : Androgenetic alopecia; AGA;
Included titles and symbols : Baldness, male pattern; MPB;
Description : Androgenetic alopecia is characterized by a loss of hair from the scalp that follows
a defined pattern (Hamilton, 1951). It occurs in women as well as in men. It is caused
by a shortening of the anagen (growth) phase and miniaturization of the hair follicle,
which results in the formation of progressively thinner, shorter hair (Bergfeld, 1995).
In men, the condition is often referred to as male pattern baldness (MPB) and appears
to be androgen-dependent (Hamilton, 1942). The condition is hereditary, and follows
a pattern that may be consistent with an autosomal dominant trait (Osborn, 1916).
Linkage evidence for an autosomal locus on 3q26 (AGA1) has been identified (Hillmer
et al., 2008). See 300710 (AGA2) for a discussion of X linkage of androgenetic alopecia.
A third locus has been found on chromosome 20p11 (AGA3; 612421).;
Inheritance : Autosomal dominant in males; recessive in females;
Prefixed ID : %109200;
Origin ID : 109200;
UMLS CUI : C4049090;
Automatic exact mappings (from CISMeF team)
DO Cross reference
False automatic mappings
HPO term(s)
Semantic type(s)
Validated automatic mappings to NTBT