Alternating esotropia
Symptom Information:
Symptom ID: | HPO:0001137 | ||
Synonyms: |
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Quality: | |||
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) Alternating esotropia(HPO:0001137) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant microcephaly | (Orphanet:2514) |
COG8-CDG | (Orphanet:95428) |
FOVEAL HYPOPLASIA 2 | (OMIM:609218) |
W syndrome | (Orphanet:2804) |