Lattice corneal dystrophy
Symptom Information:
Symptom ID: | HPO:0001149 | ||
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 cornea(HPO:0000481) Corneal dystrophy(HPO:0001131) Lattice corneal dystrophy(HPO:0001149) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1 | (OMIM:105250) |
CORNEAL DYSTROPHY, LATTICE TYPE I | (OMIM:122200) |
CORNEAL DYSTROPHY, LATTICE TYPE IIIA | (OMIM:608471) |
Familial amyloidosis, Finnish type | (Orphanet:85448) |
Familial primary localized cutaneous amyloidosis | (Orphanet:353220) |
Granular corneal dystrophy type II | (Orphanet:98963) |
Lattice corneal dystrophy type I | (Orphanet:98964) |