Hirsutism

Symptom Information:

Symptom ID: HPO:0001007
Synonyms:
Hypertrichosis [Orphanet:24040]
Hypertrichosis (disorder) [Orphanet:24040]
Excessive hair growth (finding) [Orphanet:24040]
Body hair increased [Orphanet:24040]
Hirsutism [OMIM:Hirsutism]
Hirsutism/hypertrichosis/Increased body hair [Orphanet:24040]
Hypertrichosis [MedDRA:10020864]
Hypertrichosis aggravated [MedDRA:10020864]
Hypertrichosis genital [MedDRA:10020864]
Hypertrichosis of eyelid [MedDRA:10020864]
Body hair increased [MedDRA:10020864]
Hirsutism (1 patient) [OMIM:Hirsutism (1 patient)]
Hirsutism (back and legs) [OMIM:Hirsutism (back and legs)]
Hirsutism (especially on limbs) [OMIM:Hirsutism (especially on limbs)]
Hirsutism (in some patients) [OMIM:Hirsutism (in some patients)]
Hirsutism (less common) [OMIM:Hirsutism (less common)]
Hirsutism (rare) [OMIM:Hirsutism (rare)]
Hirsutism (uncommon) [OMIM:Hirsutism (uncommon)]
Hypertrichosis (64%) [OMIM:Hypertrichosis (64%)]
Hypertrichosis (back, arms, legs) [OMIM:Hypertrichosis (back, arms, legs)]
Hypertrichosis (body, face) [OMIM:Hypertrichosis (body, face)]
Hypertrichosis (face and forehead) [OMIM:Hypertrichosis (face and forehead)]
Hypertrichosis (face, body) [OMIM:Hypertrichosis (face, body)]
Hypertrichosis (in 3 patients) [OMIM:Hypertrichosis (in 3 patients)]
Hypertrichosis (rare) [OMIM:Hypertrichosis (rare)]
Hypertrichosis (scalp, arms, legs, back) [OMIM:Hypertrichosis (scalp, arms, legs, back)]
Hirsutism [MedDRA:10020112]
Quality:
Cross references:
HPO:0004554 "Generalized hypertrichosis" [Orphanet:24040]
HPO:0000998 "Hypertrichosis" [Orphanet:24040]
HPO:0002230 "Generalized hirsutism" [Orphanet:24040]
Orphanet:24040 "Hirsutism/hypertrichosis/Increased body hair" [Orphanet:24040]
OMIM: "Hirsutism" [OMIM:Hirsutism]
OMIM: "Hirsutism (1 patient)" [OMIM:Hirsutism (1 patient)]
OMIM: "Hirsutism (back and legs)" [OMIM:Hirsutism (back and legs)]
OMIM: "Hirsutism (especially on limbs)" [OMIM:Hirsutism (especially on limbs)]
OMIM: "Hirsutism (in some patients)" [OMIM:Hirsutism (in some patients)]
OMIM: "Hirsutism (less common)" [OMIM:Hirsutism (less common)]
OMIM: "Hirsutism (rare)" [OMIM:Hirsutism (rare)]
OMIM: "Hirsutism (uncommon)" [OMIM:Hirsutism (uncommon)]
OMIM: "Hypertrichosis (64%)" [OMIM:Hypertrichosis (64%)]
OMIM: "Hypertrichosis (back, arms, legs)" [OMIM:Hypertrichosis (back, arms, legs)]
OMIM: "Hypertrichosis (body, face)" [OMIM:Hypertrichosis (body, face)]
OMIM: "Hypertrichosis (face and forehead)" [OMIM:Hypertrichosis (face and forehead)]
OMIM: "Hypertrichosis (face, body)" [OMIM:Hypertrichosis (face, body)]
OMIM: "Hypertrichosis (in 3 patients)" [OMIM:Hypertrichosis (in 3 patients)]
OMIM: "Hypertrichosis (rare)" [OMIM:Hypertrichosis (rare)]
OMIM: "Hypertrichosis (scalp, arms, legs, back)" [OMIM:Hypertrichosis (scalp, arms, legs, back)]
UMLS:C0019572 "Hirsutism" [HPO:0001007]
UMLS:C1096528 "Body hair increased" [Orphanet:24040]
UMLS:C0020555 "Hypertrichosis" [Orphanet:24040]
Is a (Direct Parents):
Orphanet Abnormality of the hair
MedDRA Hypertrichoses
HPO         Abnormal hair quantity
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)
                Abnormal hair quantity(HPO:0011362)
                   Hirsutism(HPO:0001007)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Hypertrichoses(MedDRA:10020863)
          Hirsutism(HPO:0001007)
Database Frequency: 91 / 7739
Resource:

All diseases associated with this symptom:

46,XY SEX REVERSAL 6 (OMIM:613762)
Alström syndrome (Orphanet:64)
Amaurosis - hypertrichosis (Orphanet:1021)
Atypical Mayer-Rokitansky-Küster-Hauser syndrome (Orphanet:247768)
Autosomal recessive spastic paraplegia type 53 (Orphanet:319199)
Bardet-Biedl syndrome (Orphanet:110)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Beta-thalassemia - X-linked thrombocytopenia (Orphanet:231393)
Bloom syndrome (Orphanet:125)
Bohring-Opitz syndrome (Orphanet:97297)
CEREBELLAR ATAXIA, MENTAL RETARDATION, AND DYSEQUILIBRIUM SYNDROME2 (OMIM:610185)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
COFS syndrome (Orphanet:1466)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 3 (OMIM:610759)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Carney complex (Orphanet:1359)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Cornelia de Lange syndrome (Orphanet:199)
Cortisone reductase deficiency 1 (OMIM:604931)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
Ehlers-Danlos syndrome, dermatosparaxis type (Orphanet:1901)
Epilepsy - microcephaly - skeletal dysplasia (Orphanet:1948)
FGFR2-related bent bone dysplasia (Orphanet:313855)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Floating-Harbor syndrome (Orphanet:2044)
Frontometaphyseal dysplasia (Orphanet:1826)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HYPERSECRETION OF ADRENAL ANDROGENS, FAMILIAL (OMIM:145295)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
Hennekam syndrome (Orphanet:2136)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hyperandrogenism due to cortisone reductase deficiency (Orphanet:168588)
Insulin-resistance syndrome type A (Orphanet:2297)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
KABUKI SYNDROME 1 (OMIM:147920)
KABUKI SYNDROME 2 (OMIM:300867)
Kabuki syndrome (Orphanet:2322)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA (OMIM:616342)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 (OMIM:614608)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 (OMIM:614609)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 35 (OMIM:615162)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
MGAT2-CDG (Orphanet:79329)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
OVARIAN DYSGENESIS 2 (OMIM:300510)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
POLYCYSTIC OVARY SYNDROME 1 (OMIM:184700)
Partial acquired lipodystrophy (Orphanet:79087)
Polycystic ovaries - urethral sphincter dysfunction (Orphanet:2795)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Rabson-Mendenhall syndrome (Orphanet:769)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Scheie syndrome (Orphanet:93474)
Spondyloepimetaphyseal dysplasia, Geneviève type (Orphanet:168454)
Spondyloepimetaphyseal dysplasia, Pakistani type (Orphanet:93282)
Sporadic Leigh syndrome (Orphanet:255199)
TMCO1 defect syndrome (Orphanet:228407)
Torg-Winchester syndrome (Orphanet:3460)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
Wilson-Turner syndrome (Orphanet:3459)
X-linked congenital generalized hypertrichosis (Orphanet:79495)
Zimmermann-Laband syndrome (Orphanet:3473)