Band keratopathy
Symptom Information:
Symptom ID: | HPO:0000585 | |||
Synonyms: |
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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 cornea(HPO:0000481) Corneal opacity(HPO:0007957) Opacification of the corneal stroma(HPO:0007759) Central opacification of the cornea(HPO:0011493) Band keratopathy(HPO:0000585) Abnormality of corneal stroma(HPO:0011492) Opacification of the corneal stroma(HPO:0007759) Central opacification of the cornea(HPO:0011493) Band keratopathy(HPO:0000585) MedDRA: |
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Database Frequency: | 8 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
Autosomal recessive proximal renal tubular acidosis | (Orphanet:93607) |
Blau syndrome | (Orphanet:90340) |
CORNEAL DEGENERATION, RIBBONLIKE, WITH DEAFNESS | (OMIM:121450) |
Knobloch syndrome | (Orphanet:1571) |
Proximal renal tubular acidosis | (Orphanet:47159) |