Highly arched eyebrow
Symptom Information:
Symptom ID: | HPO:0002553 | |||||||||||||||||||
Synonyms: |
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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) Highly arched eyebrow(HPO:0002553) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyebrow(HPO:0000534) Highly arched eyebrow(HPO:0002553) Abnormality of the integument(HPO:0001574) Abnormality of skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormality of the eyebrow(HPO:0000534) Highly arched eyebrow(HPO:0002553) MedDRA: |
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Database Frequency: | 92 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q11.2 microdeletion syndrome | (Orphanet:261120) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
17q12 microdeletion syndrome | (Orphanet:261265) |
17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
2q37 microdeletion syndrome | (Orphanet:1001) |
3MC SYNDROME 1 | (OMIM:257920) |
3MC SYNDROME 2 | (OMIM:265050) |
3MC SYNDROME 3 | (OMIM:248340) |
8p23.1 microduplication syndrome | (Orphanet:251076) |
8q12 microduplication syndrome | (Orphanet:228399) |
8q22.1 microdeletion syndrome | (Orphanet:178303) |
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES | (OMIM:300887) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Alpha-mannosidosis | (Orphanet:61) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
BAINBRIDGE-ROPERS SYNDROME | (OMIM:615485) |
BARAITSER-WINTER SYNDROME 2 | (OMIM:614583) |
Baraitser-Winter syndrome | (Orphanet:2995) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
CARPENTER SYNDROME 2 | (OMIM:614976) |
CHARGE syndrome | (Orphanet:138) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
CHST3-related skeletal dysplasia | (Orphanet:263463) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
CORNELIA DE LANGE SYNDROME 3 | (OMIM:610759) |
CORNELIA DE LANGE SYNDROME 4 | (OMIM:614701) |
CORNELIA DE LANGE SYNDROME 5 | (OMIM:300882) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Catel-Manzke syndrome | (Orphanet:1388) |
Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
Char syndrome | (Orphanet:46627) |
Coffin-Lowry syndrome | (Orphanet:192) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Cornelia de Lange syndrome | (Orphanet:199) |
Craniofacial-ulnar-renal syndrome | (Orphanet:293843) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Distal arthrogryposis type 5D | (Orphanet:329457) |
Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
Early infantile epileptic encephalopathy without suppression burst | (Orphanet:369894) |
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3C | (OMIM:609384) |
Facial ectodermal dysplasia | (Orphanet:1807) |
Flat face - microstomia - ear anomaly | (Orphanet:1968) |
Fucosidosis | (Orphanet:349) |
Goldberg-Shprintzen megacolon syndrome | (Orphanet:66629) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES | (OMIM:609943) |
Holoprosencephaly | (Orphanet:2162) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypertelorism, Teebi type | (Orphanet:1519) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, Birk-Barel type | (Orphanet:166108) |
Joubert syndrome | (Orphanet:475) |
Joubert syndrome 1 | (OMIM:213300) |
Joubert syndrome 14 | (OMIM:614424) |
Joubert syndrome 3 | (OMIM:608629) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with ocular defect | (Orphanet:220493) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Joubert syndrome with renal defect | (Orphanet:220497) |
Juberg-Hayward syndrome | (Orphanet:2319) |
KABUKI SYNDROME 1 | (OMIM:147920) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Kabuki syndrome | (Orphanet:2322) |
Kleefstra syndrome | (Orphanet:261494) |
Kleefstra syndrome due to 9q34 microdeletion | (Orphanet:96147) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 | (OMIM:615009) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 | (OMIM:615866) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Monosomy 9p | (Orphanet:261112) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER | (OMIM:616154) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 | (OMIM:615803) |
Pachygyria - epilepsy - intellectual deficit - dysmorphism | (Orphanet:94084) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Pseudoaminopterin syndrome | (Orphanet:221120) |
Pterygium colli - intellectual deficit - digital anomalies | (Orphanet:2988) |
Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
Qazi-Markouizos syndrome | (Orphanet:3010) |
Rubinstein-Taybi syndrome | (Orphanet:783) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
SIMOSA CRANIOFACIAL SYNDROME | (OMIM:182150) |
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia | (Orphanet:94066) |
TMCO1 defect syndrome | (Orphanet:228407) |
Temtamy preaxial brachydactyly syndrome | (Orphanet:363417) |
Temtamy syndrome | (Orphanet:1777) |
Trisomy 20p | (Orphanet:261318) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |