Exotropia

Symptom Information:

Symptom ID: HPO:0000577
Synonyms:
Exotropia [OMIM:Exotropia]
Exotropia (1 patient) [OMIM:Exotropia (1 patient)]
Exotropia (females) [OMIM:Exotropia (females)]
Exotropia (less common) [OMIM:Exotropia (less common)]
Exotropia (severe cases) [OMIM:Exotropia (severe cases)]
Quality:
Cross references:
OMIM: "Exotropia" [OMIM:Exotropia]
OMIM: "Exotropia (1 patient)" [OMIM:Exotropia (1 patient)]
OMIM: "Exotropia (females)" [OMIM:Exotropia (females)]
OMIM: "Exotropia (less common)" [OMIM:Exotropia (less common)]
OMIM: "Exotropia (severe cases)" [OMIM:Exotropia (severe cases)]
UMLS:C0015310 "Exotropia" [HPO:0000577]
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)
                      Exotropia(HPO:0000577)
MedDRA:
Database Frequency: 43 / 7739
Resource:

All diseases associated with this symptom:

2-methylbutyryl-CoA dehydrogenase deficiency (Orphanet:79157)
22q11.2 deletion syndrome (Orphanet:567)
5p13 microduplication syndrome (Orphanet:329802)
Angelman syndrome (Orphanet:72)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bilateral frontoparietal polymicrogyria (Orphanet:101070)
COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE (OMIM:216820)
CUTIS VERTICIS GYRATA, RETINITIS PIGMENTOSA, AND SENSORINEURAL DEAFNESS (OMIM:605685)
Carpenter-Waziri syndrome (Orphanet:93973)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Congenital fibrosis of extraocular muscles (Orphanet:45358)
Craniofrontonasal dysplasia (Orphanet:1520)
DIGEORGE SYNDROME (OMIM:188400)
DPAGT1-CDG (Orphanet:86309)
Distal monosomy 6p (Orphanet:96125)
FACIOCARDIOMELIC SYNDROME (OMIM:612731)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2 (OMIM:602078)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, WITH SYNERGISTIC DIVERGENCE (OMIM:609612)
Holmes-Gang syndrome (Orphanet:93970)
Hurler syndrome (Orphanet:93473)
Intellectual deficit, X-linked, Miles-Carpenter type (Orphanet:85283)
Juberg-Marsidi syndrome (Orphanet:93972)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Langer-Giedion syndrome (Orphanet:502)
Leber plus disease (Orphanet:99718)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Marfan syndrome type 1 (Orphanet:284963)
Moebius syndrome (Orphanet:570)
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:616263)
Neuroectodermal melanolysosomal disease (Orphanet:33445)
OPHTHALMOPLEGIA, FAMILIAL TOTAL, WITH IRIS TRANSILLUMINATION (OMIM:165098)
Oculofaciocardiodental syndrome (Orphanet:2712)
PORENCEPHALY 1 (OMIM:175780)
Porencephaly (Orphanet:2940)
RIENHOFF SYNDROME (OMIM:615582)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Salla disease (Orphanet:309334)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Wolfram syndrome 1 (OMIM:222300)
X-linked creatine transporter deficiency (Orphanet:52503)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)