Esotropia

Symptom Information:

Symptom ID: HPO:0000565
Synonyms:
Convergent strabismus [HPO:0000565]
Convergent strabismus [OMIM:Convergent strabismus]
Esotropia [OMIM:Esotropia]
Esotropia (1 patient) [OMIM:Esotropia (1 patient)]
Esotropia (about half of patients) [OMIM:Esotropia (about half of patients)]
Esotropia (in some patients) [OMIM:Esotropia (in some patients)]
Strabismus convergens [IBIS,cm]
Quality:
Cross references:
OMIM: "Convergent strabismus" [OMIM:Convergent strabismus]
OMIM: "Esotropia" [OMIM:Esotropia]
OMIM: "Esotropia (1 patient)" [OMIM:Esotropia (1 patient)]
OMIM: "Esotropia (about half of patients)" [OMIM:Esotropia (about half of patients)]
OMIM: "Esotropia (in some patients)" [OMIM:Esotropia (in some patients)]
Is a (Direct Parents):
HPO         Strabismus
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:
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)