Thick eyebrow

Symptom Information:

Symptom ID: HPO:0000574
Synonyms:
Bushy eyebrows [HPO:0000574]
Dense eyebrow [HPO:0000574]
Heavy eyebrows [HPO:0000574]
Hypertrichosis of the eyebrow [HPO:0000574]
HYPERTRICHOSIS OF THE EYEBROWS [HPO:0000574]
Prominent eyebrows [HPO:0000574]
Thick eyebrows [HPO:0000574]
Bushy eyebrows [OMIM:Bushy eyebrows]
Heavy eyebrows [OMIM:Heavy eyebrows]
Hypertrichosis of the eyebrows [OMIM:Hypertrichosis of the eyebrows]
Prominent eyebrows [OMIM:Prominent eyebrows]
Thick eyebrows [OMIM:Thick eyebrows]
Thick/bushy eyebrows [Orphanet:6200]
Thick eyebrows (in some patients) [OMIM:Thick eyebrows (in some patients)]
Quality:
Cross references:
Orphanet:6200 "Thick/bushy eyebrows" [Orphanet:6200]
OMIM: "Bushy eyebrows" [OMIM:Bushy eyebrows]
OMIM: "Heavy eyebrows" [OMIM:Heavy eyebrows]
OMIM: "Hypertrichosis of the eyebrows" [OMIM:Hypertrichosis of the eyebrows]
OMIM: "Prominent eyebrows" [OMIM:Prominent eyebrows]
OMIM: "Thick eyebrows" [OMIM:Thick eyebrows]
OMIM: "Thick eyebrows (in some patients)" [OMIM:Thick eyebrows (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the eyebrow
Orphanet Abnormality of the eyebrow
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 the eyebrow(HPO:0000534)
                   Thick eyebrow(HPO:0000574)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyebrow(HPO:0000534)
                      Thick eyebrow(HPO:0000574)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyebrow(HPO:0000534)
                      Thick eyebrow(HPO:0000574)
MedDRA:
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
17q21.31 microduplication syndrome (Orphanet:217340)
2q23.1 microdeletion syndrome (Orphanet:228402)
3M syndrome (Orphanet:2616)
5q14.3 microdeletion syndrome (Orphanet:228384)
Acromegaloid facial appearance syndrome (Orphanet:965)
Acroosteolysis, dominant type (Orphanet:955)
Alpha-mannosidosis (Orphanet:61)
Amaurosis - hypertrichosis (Orphanet:1021)
Amelogenesis imperfecta and gingival hyperplasia syndrome (Orphanet:171836)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
COFFIN-SIRIS SYNDROME (OMIM:135900)
CORNELIA DE LANGE SYNDROME 2 (OMIM:300590)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
Cataract - deafness - hypogonadism (Orphanet:1383)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Char syndrome (Orphanet:46627)
Christianson syndrome (Orphanet:85278)
Coffin-Lowry syndrome (Orphanet:192)
Coffin-Siris syndrome (Orphanet:1465)
Cohen syndrome (Orphanet:193)
Cornelia de Lange syndrome (Orphanet:199)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Distal monosomy 19p13.3 (Orphanet:96129)
EEC syndrome (Orphanet:1896)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 (OMIM:615859)
Fabry disease (Orphanet:324)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Familial osteodysplasia, Anderson type (Orphanet:2769)
Fountain syndrome (Orphanet:3219)
Fucosidosis (Orphanet:349)
Gingival fibromatosis - facial dysmorphism (Orphanet:2025)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
Holoprosencephaly (Orphanet:2162)
Hurler syndrome (Orphanet:93473)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Hypertrichosis lanuginosa congenita (Orphanet:2222)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit, Birk-Barel type (Orphanet:166108)
Intellectual deficit, X-linked, Stevenson type (Orphanet:85325)
KBG syndrome (Orphanet:2332)
Langer-Giedion syndrome (Orphanet:502)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 (OMIM:614608)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 (OMIM:614609)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45 (OMIM:615979)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM (OMIM:606242)
MGAT2-CDG (Orphanet:79329)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Marden-Walker syndrome (Orphanet:2461)
Marshall-Smith syndrome (Orphanet:561)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Monosomy 22q13 (Orphanet:48652)
Monosomy 9p (Orphanet:261112)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Mucopolysaccharidosis type 2 (Orphanet:580)
Multiple endocrine neoplasia type 2B (Orphanet:247709)
Multiple sulfatase deficiency (Orphanet:585)
Myhre syndrome (Orphanet:2588)
Non-distal trisomy 13q (Orphanet:1702)
Oculofaciocardiodental syndrome (Orphanet:2712)
Oliver syndrome (Orphanet:2920)
Progeroid syndrome, Petty type (Orphanet:2963)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Rabson-Mendenhall syndrome (Orphanet:769)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
SLC35A2-CDG (Orphanet:356961)
Sanfilippo syndrome type D (Orphanet:79272)
Scheie syndrome (Orphanet:93474)
Shoulder and girdle defects - familial intellectual deficit (Orphanet:2580)
Spondyloepimetaphyseal dysplasia, Bieganski type (Orphanet:168448)
Synostosis - microcephaly - scoliosis (Orphanet:3268)
TENORIO SYNDROME (OMIM:616260)
TMCO1 defect syndrome (Orphanet:228407)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Trisomy 12p (Orphanet:1699)
Trisomy 20p (Orphanet:261318)
Trisomy 4p (Orphanet:1738)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 3 (Orphanet:896)
Wiedemann-Steiner syndrome (Orphanet:319182)
Wilson-Turner syndrome (Orphanet:3459)
Zimmermann-Laband syndrome (Orphanet:3473)