Sparse axillary hair

Symptom Information:

Symptom ID: HPO:0002215
Synonyms:
Sparse axillary and pubic hair [HPO:0002215]
Sparse scalp, axillary, and pubic hair [HPO:0002215]
sparse to absent axillary hair [HPO:0002215]
Decreased axillary hair [Orphanet:24120]
Sparse axillary and pubic hair [OMIM:Sparse axillary and pubic hair]
Sparse axillary hair [OMIM:Sparse axillary hair]
Sparse scalp, axillary, and pubic hair [OMIM:Sparse scalp, axillary, and pubic hair]
Sparse to absent axillary hair [OMIM:Sparse to absent axillary hair]
Decreased body hair/axillar/pubic hairlessness [Orphanet:24120]
Axillary and pubic hair sparse [OMIM:Axillary and pubic hair sparse]
Sparse to absent axillary hair (in some patients) [OMIM:Sparse to absent axillary hair (in some patients)]
Quality:
Cross references:
Orphanet:24120 "Decreased body hair/axillar/pubic hairlessness" [Orphanet:24120]
OMIM: "Sparse axillary and pubic hair" [OMIM:Sparse axillary and pubic hair]
OMIM: "Sparse axillary hair" [OMIM:Sparse axillary hair]
OMIM: "Sparse scalp, axillary, and pubic hair" [OMIM:Sparse scalp, axillary, and pubic hair]
OMIM: "Sparse to absent axillary hair" [OMIM:Sparse to absent axillary hair]
OMIM: "Axillary and pubic hair sparse" [OMIM:Axillary and pubic hair sparse]
OMIM: "Sparse to absent axillary hair (in some patients)" [OMIM:Sparse to absent axillary hair (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the axillary hair
HPO         Sparse hair
Orphanet Abnormality of the hair
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormality of hair density(HPO:0011357)
                   Sparse hair(HPO:0008070)
                      Sparse axillary hair(HPO:0002215)
                Abnormality of secondary sexual hair(HPO:0009888)
                   Abnormality of the axillary hair(HPO:0100134)
                      Sparse axillary hair(HPO:0002215)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

46,XY SEX REVERSAL 6 (OMIM:613762)
ADULT syndrome (Orphanet:978)
ANDROGEN INSENSITIVITY SYNDROME (OMIM:300068)
AREDYLD syndrome (Orphanet:1133)
Complete androgen insensitivity syndrome (Orphanet:99429)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA (OMIM:228300)
HYPOTRICHOSIS 8 (OMIM:278150)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary hypotrichosis with recurrent skin vesicles (Orphanet:217407)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hurler-Scheie syndrome (Orphanet:93476)
Hypotrichosis simplex (Orphanet:55654)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
Normosmic congenital hypogonadotropic hypogonadism (Orphanet:432)
Oculotrichodysplasia (Orphanet:2718)
Trichodysplasia - xeroderma (Orphanet:3361)
Ulnar-mammary syndrome (Orphanet:3138)
Woodhouse-Sakati syndrome (Orphanet:3464)