Congenital fibrosis of extraocular muscles
Symptom Information:
Symptom ID: | HPO:0001491 | |||||||
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 morphology(HPO:0012372) Abnormality of the extraocular muscles(HPO:0008049) Congenital fibrosis of extraocular muscles(HPO:0001491) MedDRA: |
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Database Frequency: | 9 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Bilateral frontal polymicrogyria | (Orphanet:208444) |
Congenital fibrosis of extraocular muscles | (Orphanet:45358) |
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1 | (OMIM:135700) |
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, 3C | (OMIM:609384) |
Moebius syndrome | (Orphanet:570) |
Polymicrogyria due to TUBB2B mutation | (Orphanet:300573) |
TUKEL SYNDROME | (OMIM:609428) |