Esotropia
Symptom Information:
Symptom ID: | HPO:0000565 | |||||||
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 the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Abnormality of eye movement(HPO:0000496) Abnormal conjugate eye movement(HPO:0000549) Strabismus(HPO:0000486) Esotropia(HPO:0000565) MedDRA: |
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Database Frequency: | 58 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
ADAMS-OLIVER SYNDROME 1 | (OMIM:100300) |
AICA-ribosiduria | (Orphanet:250977) |
ASYMMETRIC SHORT STATURE SYNDROME | (OMIM:108450) |
Acromelanosis | (Orphanet:39) |
Adams-Oliver syndrome | (Orphanet:974) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome | (Orphanet:363429) |
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency | (Orphanet:324262) |
Bilateral frontoparietal polymicrogyria | (Orphanet:101070) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
CAMOS syndrome | (Orphanet:83472) |
CHROMOSOME 5q12 DELETION SYNDROME | (OMIM:615668) |
COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE | (OMIM:216820) |
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital fibrosis of extraocular muscles | (Orphanet:45358) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Craniolenticulosutural dysplasia | (Orphanet:50814) |
FACIAL PARESIS, HEREDITARY CONGENITAL, 3 | (OMIM:614744) |
Femoral-facial syndrome | (Orphanet:1988) |
Gaucher disease type 2 | (Orphanet:77260) |
HYPEREKPLEXIA 2 | (OMIM:614619) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
Intellectual deficit, X-linked, Cantagrel type | (Orphanet:85277) |
Intellectual disability-strabismus syndrome | (Orphanet:363528) |
Joubert syndrome 2 | (OMIM:608091) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS | (OMIM:613671) |
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES | (OMIM:606772) |
MICROPHTHALMIA, SYNDROMIC 13 | (OMIM:300915) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marshall syndrome | (Orphanet:560) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Moebius syndrome | (Orphanet:570) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Neonatal adrenoleukodystrophy | (Orphanet:44) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
OROFACIODIGITAL SYNDROME VI | (OMIM:277170) |
PACHYGYRIA, FRONTOTEMPORAL | (OMIM:610279) |
PEROXISOME BIOGENESIS DISORDER 2B | (OMIM:202370) |
PMM2-CDG | (Orphanet:79318) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 | (OMIM:615803) |
Pigmented paravenous retinochoroidal atrophy | (Orphanet:251295) |
Pontocerebellar hypoplasia type 8 | (Orphanet:324569) |
Prader-Willi syndrome | (Orphanet:739) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Radial ray hypoplasia - choanal atresia | (Orphanet:3026) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
SCLEROSTEOSIS 1 | (OMIM:269500) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 | (OMIM:616204) |
Sclerosteosis | (Orphanet:3152) |
Timothy syndrome | (Orphanet:65283) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
XIA-GIBBS SYNDROME | (OMIM:615829) |