Sparse pubic hair
Symptom Information:
Symptom ID: | HPO:0002225 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |