Lattice corneal dystrophy

Symptom Information:

Symptom ID: HPO:0001149
Synonyms:
Lattice corneal dystrophy [OMIM:Lattice corneal dystrophy]
Quality:
Cross references:
OMIM: "Lattice corneal dystrophy" [OMIM:Lattice corneal dystrophy]
Is a (Direct Parents):
HPO         Corneal dystrophy
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:
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)