Hypertrichosis

Symptom Information:

Symptom ID: HPO:0000998
Synonyms:
Hypertrichosis (disorder) [Orphanet:24040]
Excessive hair growth (finding) [Orphanet:24040]
Body hair increased [Orphanet:24040]
Hypertrichosis [Orphanet:24040]
Hypertrichosis [OMIM:Hypertrichosis]
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]
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)]
Quality:
Cross references:
HPO:0004554 "Generalized hypertrichosis" [Orphanet:24040]
HPO:0001007 "Hirsutism" [Orphanet:24040]
HPO:0002230 "Generalized hirsutism" [Orphanet:24040]
Orphanet:24040 "Hirsutism/hypertrichosis/Increased body hair" [Orphanet:24040]
OMIM: "Hypertrichosis" [OMIM:Hypertrichosis]
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:C0020555 "Hypertrichosis" [HPO:0000998]
UMLS:C1096528 "Body hair increased" [Orphanet:24040]
UMLS:C0020555 "Hypertrichosis" [Orphanet:24040]
Is a (Direct Parents):
MedDRA Hypertrichoses
Orphanet Abnormality of the hair
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)
                   Hypertrichosis(HPO:0000998)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Hypertrichoses(MedDRA:10020863)
          Hypertrichosis(HPO:0000998)
Database Frequency: 52 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
Adducted thumbs - arthrogryposis, Christian type (Orphanet:2952)
Alpha-mannosidosis (Orphanet:61)
Alström syndrome (Orphanet:64)
Autosomal recessive spastic paraplegia type 53 (Orphanet:319199)
Barber-Say syndrome (Orphanet:1231)
Bardet-Biedl syndrome (Orphanet:110)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bloom syndrome (Orphanet:125)
Carney complex (Orphanet:1359)
Congenital erythropoietic porphyria (Orphanet:79277)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital reticular ichthyosiform erythroderma (Orphanet:281190)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Filippi syndrome (Orphanet:3255)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
Hurler syndrome (Orphanet:93473)
Insulin-resistance syndrome type A (Orphanet:2297)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
Leigh syndrome (Orphanet:506)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 (OMIM:615866)
Marshall-Smith syndrome (Orphanet:561)
Morgagni-Stewart-Morel syndrome (Orphanet:77296)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
PORPHYRIA CUTANEA TARDA, TYPE I (OMIM:176090)
Partial acquired lipodystrophy (Orphanet:79087)
Polycystic ovaries - urethral sphincter dysfunction (Orphanet:2795)
Pontocerebellar hypoplasia type 8 (Orphanet:324569)
Porphyria cutanea tarda (Orphanet:101330)
Rabson-Mendenhall syndrome (Orphanet:769)
Ramon syndrome (Orphanet:3019)
SRD5A3-CDG (Orphanet:324737)
Schinzel-Giedion syndrome (Orphanet:798)
Sporadic Leigh syndrome (Orphanet:255199)
TENORIO SYNDROME (OMIM:616260)
TMCO1 defect syndrome (Orphanet:228407)
Transaldolase deficiency (Orphanet:101028)
Wilson-Turner syndrome (Orphanet:3459)
Zimmermann-Laband syndrome (Orphanet:3473)