Highly arched eyebrow

Symptom Information:

Symptom ID: HPO:0002553
Synonyms:
Arched eyebrows [HPO:0002553]
Bowed and upward slanting eyebrows [HPO:0002553]
Broad, arched eyebrows [HPO:0002553]
HIGH ARCHED EYEBROWS [HPO:0002553]
High, rounded eyebrows [HPO:0002553]
High-arched eyebrows [HPO:0002553]
Thick, flared eyebrows [HPO:0002553]
Arched eyebrows [OMIM:Arched eyebrows]
Bowed and upward slanting eyebrows [OMIM:Bowed and upward slanting eyebrows]
Broad, arched eyebrows [OMIM:Broad, arched eyebrows]
High arched eyebrows [OMIM:High arched eyebrows]
High, rounded eyebrows [OMIM:High, rounded eyebrows]
High-arched eyebrows [OMIM:High-arched eyebrows]
Thick, flared eyebrows [OMIM:Thick, flared eyebrows]
High arched eyebrows [Orphanet:6400]
Arched eyebrows (1/4 patients) [OMIM:Arched eyebrows (1/4 patients)]
Arched eyebrows (in some patients) [OMIM:Arched eyebrows (in some patients)]
High-rounded eyebrows [OMIM:High-rounded eyebrows]
Highly arched eyebrows [OMIM:Highly arched eyebrows]
Quality:
Cross references:
Orphanet:6400 "High arched eyebrows" [Orphanet:6400]
OMIM: "Arched eyebrows" [OMIM:Arched eyebrows]
OMIM: "Bowed and upward slanting eyebrows" [OMIM:Bowed and upward slanting eyebrows]
OMIM: "Broad, arched eyebrows" [OMIM:Broad, arched eyebrows]
OMIM: "High arched eyebrows" [OMIM:High arched eyebrows]
OMIM: "High, rounded eyebrows" [OMIM:High, rounded eyebrows]
OMIM: "High-arched eyebrows" [OMIM:High-arched eyebrows]
OMIM: "Thick, flared eyebrows" [OMIM:Thick, flared eyebrows]
OMIM: "Arched eyebrows (1/4 patients)" [OMIM:Arched eyebrows (1/4 patients)]
OMIM: "Arched eyebrows (in some patients)" [OMIM:Arched eyebrows (in some patients)]
OMIM: "High-rounded eyebrows" [OMIM:High-rounded eyebrows]
OMIM: "Highly arched eyebrows" [OMIM:Highly arched eyebrows]
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)
                   Highly arched eyebrow(HPO:0002553)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyebrow(HPO:0000534)
                      Highly arched eyebrow(HPO:0002553)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyebrow(HPO:0000534)
                      Highly arched eyebrow(HPO:0002553)
MedDRA:
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)