Peters anomaly
Symptom Information:
Symptom ID: | HPO:0000659 | |||||
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 morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the anterior chamber(HPO:0000593) Anterior segment dysgenesis(HPO:0007700) Peters anomaly(HPO:0000659) MedDRA: |
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Database Frequency: | 10 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
17q12 microduplication syndrome | (Orphanet:261272) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Isolated aniridia | (Orphanet:250923) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 | (OMIM:614643) |
Muscle-eye-brain disease | (Orphanet:588) |
Peters anomaly | (Orphanet:708) |
Peters-plus syndrome | (Orphanet:709) |
Subaortic stenosis - short stature | (Orphanet:3191) |