Exotropia
Symptom Information:
Symptom ID: | HPO:0000577 | ||||||
Synonyms: |
|
||||||
Quality: | |||||||
Cross references: |
|
||||||
Is a (Direct Parents): |
|
||||||
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) |