Telecanthus
Symptom Information:
Symptom ID: | HPO:0000506 | |||||||||
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) Abnormality of the periorbital region(HPO:0000606) Abnormality of the eyelid(HPO:0000492) Telecanthus(HPO:0000506) obsolete Abnormality of the ocular region(HPO:0000284) Abnormality of the eyelid(HPO:0000492) Telecanthus(HPO:0000506) MedDRA: |
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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) |