Sparse pubic hair

Symptom Information:

Symptom ID: HPO:0002225
Synonyms:
Decreased sexual hair [HPO:0002225]
sparse to absent pubic hair [HPO:0002225]
Decreased pubic hair [Orphanet:24120]
Decreased sexual hair [OMIM:Decreased sexual hair]
Sparse pubic hair [OMIM:Sparse pubic hair]
Sparse to absent pubic hair [OMIM:Sparse to absent pubic hair]
Decreased body hair/axillar/pubic hairlessness [Orphanet:24120]
Quality:
Cross references:
Orphanet:24120 "Decreased body hair/axillar/pubic hairlessness" [Orphanet:24120]
OMIM: "Decreased sexual hair" [OMIM:Decreased sexual hair]
OMIM: "Sparse pubic hair" [OMIM:Sparse pubic hair]
OMIM: "Sparse to absent pubic hair" [OMIM:Sparse to absent pubic hair]
Is a (Direct Parents):
HPO         Abnormality of the pubic hair
Orphanet Abnormality of the hair
Orphanet Sparse axillary hair
HPO         Sparse 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 pubic hair(HPO:0002225)
                Abnormality of secondary sexual hair(HPO:0009888)
                   Abnormality of the pubic hair(HPO:0100133)
                      Sparse pubic hair(HPO:0002225)
MedDRA:
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

46,XY complete gonadal dysgenesis (Orphanet:242)
ANDROGEN INSENSITIVITY SYNDROME (OMIM:300068)
AREDYLD syndrome (Orphanet:1133)
Adiposis dolorosa (Orphanet:36397)
Albright hereditary osteodystrophy (Orphanet:665)
Alopecia (Orphanet:79364)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alopecia antibody deficiency (Orphanet:1006)
Alopecia universalis (Orphanet:701)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Androgen insensitivity syndrome (Orphanet:754)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive palmoplantar keratoderma and congenital alopecia (Orphanet:1366)
BRESEK syndrome (Orphanet:85284)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Bullous dystrophy, macular type (Orphanet:1867)
CHILD syndrome (Orphanet:139)
Complete androgen insensitivity syndrome (Orphanet:99429)
Crandall syndrome (Orphanet:202)
Cronkhite-Canada syndrome (Orphanet:2930)
Dermo-odonto dysplasia (Orphanet:1660)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
GAPO syndrome (Orphanet:2067)
Graham Little-Piccardi-Lassueur syndrome (Orphanet:505)
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA (OMIM:308700)
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA (OMIM:228300)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hallermann-Streiff syndrome (Orphanet:2108)
Hemochromatosis, type 2A (OMIM:602390)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hurler-Scheie syndrome (Orphanet:93476)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypogonadism - mitral valve prolapse - intellectual deficit (Orphanet:2233)
Hypogonadotropic hypogonadism - frontoparietal alopecia (Orphanet:2230)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis simplex (Orphanet:55654)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA (OMIM:308750)
KID syndrome (Orphanet:477)
Lamellar ichthyosis (Orphanet:313)
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies (Orphanet:2234)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Normosmic congenital hypogonadotropic hypogonadism (Orphanet:432)
ONYCHOTRICHODYSPLASIA AND NEUTROPENIA (OMIM:258360)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odontotrichomelic syndrome (Orphanet:2723)
POEMS syndrome (Orphanet:2905)
Pachydermoperiostosis (Orphanet:2796)
Papillon-Lefèvre syndrome (Orphanet:678)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Syndromic X-linked intellectual deficit 7 (Orphanet:85274)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Trichodysplasia - xeroderma (Orphanet:3361)
Ulnar-mammary syndrome (Orphanet:3138)
Weaver-Williams syndrome (Orphanet:3448)
Woodhouse-Sakati syndrome (Orphanet:3464)
Woolly hair (Orphanet:170)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Xq27.3q28 duplication syndrome (Orphanet:261483)