Telecanthus

Symptom Information:

Symptom ID: HPO:0000506
Synonyms:
Dystopia canthorum [HPO:0000506]
Telecanthus (finding) [Orphanet:7250]
Telecanthus [Orphanet:7250]
Dystopia canthorum [OMIM:Dystopia canthorum]
Telecanthus [OMIM:Telecanthus]
Telecanthus/canthal dystopy [Orphanet:7250]
Telecanthus (females) [OMIM:Telecanthus (females)]
Telecanthus (in 1 family) [OMIM:Telecanthus (in 1 family)]
Telecanthus (in some patients) [OMIM:Telecanthus (in some patients)]
Quality:
Cross references:
Orphanet:7250 "Telecanthus/canthal dystopy" [Orphanet:7250]
OMIM: "Dystopia canthorum" [OMIM:Dystopia canthorum]
OMIM: "Telecanthus" [OMIM:Telecanthus]
OMIM: "Telecanthus (females)" [OMIM:Telecanthus (females)]
OMIM: "Telecanthus (in 1 family)" [OMIM:Telecanthus (in 1 family)]
OMIM: "Telecanthus (in some patients)" [OMIM:Telecanthus (in some patients)]
UMLS:C0423113 "Telecanthus" [HPO:0000506]
UMLS:C0423113 "Telecanthus" [Orphanet:7250]
Is a (Direct Parents):
HPO         Abnormality of the eyelid
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 eyelid(HPO:0000492)
                      Telecanthus(HPO:0000506)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyelid(HPO:0000492)
                      Telecanthus(HPO:0000506)
MedDRA:
Database Frequency: 156 / 7739
Resource:

All diseases associated with this symptom:

1q44 microdeletion syndrome (Orphanet:238769)
22q11.2 deletion syndrome (Orphanet:567)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
8q12 microduplication syndrome (Orphanet:228399)
8q22.1 microdeletion syndrome (Orphanet:178303)
AREDYLD syndrome (Orphanet:1133)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
AXENFELD-RIEGER ANOMALY WITH PARTIALLY ABSENT EYE MUSCLES, DISTINCTIVEFACE, HYDROCEPHALY, AND SKELETAL ABNORMALITIES (OMIM:109120)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Acrocraniofacial dysostosis (Orphanet:949)
Acromelic frontonasal dysplasia (Orphanet:1827)
Acroosteolysis, dominant type (Orphanet:955)
Alar cartilages hypoplasia - coloboma - telecanthus (Orphanet:2007)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive spastic paraplegia type 54 (Orphanet:320380)
Axenfeld-Rieger syndrome (Orphanet:782)
Axial spondylometaphyseal dysplasia (Orphanet:168549)
Baraitser-Winter syndrome (Orphanet:2995)
Barber-Say syndrome (Orphanet:1231)
Bencze syndrome (Orphanet:1241)
Blepharonasofacial malformation syndrome (Orphanet:1252)
Blepharophimosis - epicanthus inversus - ptosis (Orphanet:126)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
Branchio-oculo-facial syndrome (Orphanet:1297)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CARDIOFACIOCUTANEOUS SYNDROME 4 (OMIM:615280)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Carpenter syndrome (Orphanet:65759)
Chondrodysplasia - disorder of sex development (Orphanet:1422)
Cleft palate - stapes fixation - oligodontia (Orphanet:2010)
Coffin-Lowry syndrome (Orphanet:192)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniometaphyseal dysplasia (Orphanet:1522)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Cutis laxa (Orphanet:209)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Distal monosomy 3p (Orphanet:1620)
Dubowitz syndrome (Orphanet:235)
Dysmorphism - pectus carinatum - joint laxity (Orphanet:2104)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
EEC syndrome (Orphanet:1896)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 (OMIM:615859)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Endomyocardial fibroelastosis (Orphanet:2022)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
FETAL AKINESIA SYNDROME, X-LINKED (OMIM:300073)
FRONTOFACIONASAL DYSPLASIA (OMIM:229400)
Facial dysmorphism - shawl scrotum - joint laxity (Orphanet:1778)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Familial lambdoid synostosis (Orphanet:3267)
Fetal akinesia deformation sequence (Orphanet:994)
Fetal alcohol syndrome (Orphanet:1915)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Floating-Harbor syndrome (Orphanet:2044)
Freeman-Sheldon syndrome (Orphanet:2053)
Fronto-facio-nasal dysostosis (Orphanet:1791)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Gorlin syndrome (Orphanet:377)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Gómez-López-Hernández syndrome (Orphanet:1532)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hallermann-Streiff syndrome (Orphanet:2108)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Hypoglossia - hypodactyly (Orphanet:989)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit, X-linked - short stature - obesity (Orphanet:3055)
Jacobsen syndrome (Orphanet:2308)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
KBG syndrome (Orphanet:2332)
LAMBOTTE SYNDROME (OMIM:245552)
LIG4 syndrome (Orphanet:99812)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Linear nevus sebaceus syndrome (Orphanet:2612)
Lymphedema - atrial septal defects - facial changes (Orphanet:86915)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 (OMIM:616158)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES (OMIM:606772)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marden-Walker syndrome (Orphanet:2461)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Mesomelia-synostoses syndrome (Orphanet:2496)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome (Orphanet:369970)
Mowat-Wilson syndrome (Orphanet:2152)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Native American myopathy (Orphanet:168572)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
OROFACIODIGITAL SYNDROME XIV (OMIM:615948)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Orofaciodigital syndrome type 9 (Orphanet:141007)
PACHYGYRIA, FRONTOTEMPORAL (OMIM:610279)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
POLYCYSTIC KIDNEY DISEASE, POTTER TYPE I, WITH MICROBRACHYCEPHALY,HYPERTELORISM, AND BRACHYMELIA (OMIM:263210)
Pai syndrome (Orphanet:1993)
Pitt-Hopkins-like syndrome 2 (OMIM:614325)
Potocki-Shaffer syndrome (Orphanet:52022)
Prader-Willi syndrome (Orphanet:739)
Ptosis - upper ocular movement limitation - absence of lacrimal punctum (Orphanet:228396)
Ring chromosome 1 (Orphanet:1437)
Rubinstein-Taybi syndrome (Orphanet:783)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
SHORT syndrome (Orphanet:3163)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
Scalp-ear-nipple syndrome (Orphanet:2036)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Stickler syndrome (Orphanet:828)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
TELECANTHUS (OMIM:187350)
TENORIO SYNDROME (OMIM:616260)
TRISOMY 18-LIKE SYNDROME (OMIM:601161)
Telecanthus - hypertelorism - strabismus - pes cavus (Orphanet:3293)
Temtamy syndrome (Orphanet:1777)
Tetrasomy 12p (Orphanet:884)
Toriello-Carey syndrome (Orphanet:3338)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Velo-facial-skeletal syndrome (Orphanet:3424)
W syndrome (Orphanet:2804)
WAARDENBURG SYNDROME, TYPE 2D (OMIM:608890)
WHISTLING FACE SYNDROME, RECESSIVE FORM (OMIM:277720)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
Waardenburg syndrome type 3 (Orphanet:896)
Waardenburg-Shah syndrome (Orphanet:897)
X-linked Opitz G/BBB syndrome (Orphanet:306597)