Thick eyebrow
Symptom Information:
Symptom ID: | HPO:0000574 | ||||||||||||||
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 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) 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) MedDRA: |
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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) |