Corneal dystrophy

Symptom Information:

Symptom ID: HPO:0001131
Synonyms:
Hereditary corneal dystrophy (disorder) [Orphanet:4500]
Corneal dystrophy (disorder) [Orphanet:4500]
Corneal dystrophy [Orphanet:4500]
Hereditary corneal dystrophy [Orphanet:4500]
Corneal dystrophy [OMIM:Corneal dystrophy]
Hereditary corneal dystrophy, unspecified [Orphanet:4500]
Corneal dystrophy [MedDRA:10011005]
Endothelial corneal dystrophy [MedDRA:10011005]
Granular corneal dystrophy [MedDRA:10011005]
Hereditary corneal dystrophies [MedDRA:10011005]
Hereditary corneal dystrophy, unspecified [MedDRA:10011005]
Juvenile epithelial corneal dystrophy [MedDRA:10011005]
Lattice corneal dystrophy [MedDRA:10011005]
Macular corneal dystrophy [MedDRA:10011005]
Other anterior corneal dystrophies [MedDRA:10011005]
Other posterior corneal dystrophies [MedDRA:10011005]
Other stromal corneal dystrophies [MedDRA:10011005]
Fuchs' endothelial dystrophy [MedDRA:10011005]
Anterior membrane dystrophy [MedDRA:10011005]
Cogan's dystrophy [MedDRA:10011005]
Map dot fingerprint dystrophy [MedDRA:10011005]
Meesman's dystrophy [MedDRA:10011005]
Congenital corneal dystrophy [MedDRA:10011005]
Corneal guttata [MedDRA:10011005]
Corneal dystrophy (onset early in childhood) [OMIM:Corneal dystrophy (onset early in childhood)]
Corneal endothelial dystrophy (guttata) [OMIM:Corneal endothelial dystrophy (guttata)]
Corneal endothelial dystrophy (in some patients) [OMIM:Corneal endothelial dystrophy (in some patients)]
Macular corneal dystrophy [OMIM:Macular corneal dystrophy]
Quality:
Cross references:
Orphanet:4500 "Corneal dystrophy" [Orphanet:4500]
OMIM: "Corneal dystrophy" [OMIM:Corneal dystrophy]
OMIM: "Corneal dystrophy (onset early in childhood)" [OMIM:Corneal dystrophy (onset early in childhood)]
OMIM: "Corneal endothelial dystrophy (guttata)" [OMIM:Corneal endothelial dystrophy (guttata)]
OMIM: "Corneal endothelial dystrophy (in some patients)" [OMIM:Corneal endothelial dystrophy (in some patients)]
OMIM: "Macular corneal dystrophy" [OMIM:Macular corneal dystrophy]
UMLS:C0010036 "Corneal dystrophy" [Orphanet:4500]
UMLS:C0010035 "Hereditary corneal dystrophy" [Orphanet:4500]
Is a (Direct Parents):
MedDRA Corneal and scleral disorders congenital
Orphanet Abnormality of the eye
HPO         Abnormality of the cornea
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)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Corneal and scleral disorders congenital(MedDRA:10010987)
          Corneal dystrophy(HPO:0001131)
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

Alagille syndrome (Orphanet:52)
Alport syndrome (Orphanet:63)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Blue cone monochromatism (Orphanet:16)
Brittle cornea syndrome (Orphanet:90354)
CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS (OMIM:121390)
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 2 (OMIM:610158)
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 4 (OMIM:613268)
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 6 (OMIM:613270)
CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 8 (OMIM:615523)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2 (OMIM:609140)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 3 (OMIM:609141)
Cataract-microcornea syndrome (Orphanet:1377)
Central cloudy dystrophy of Francois (Orphanet:98972)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Corneal anesthesia - deafness - intellectual deficit (Orphanet:1051)
Corneal dystrophy - perceptive deafness (Orphanet:1490)
Corneal-cerebellar syndrome (Orphanet:3177)
Dermochondrocorneal dystrophy (Orphanet:79149)
EDICT syndrome (Orphanet:293936)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectopia lentis - chorioretinal dystrophy - myopia (Orphanet:1884)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Fabry disease (Orphanet:324)
Fuchs endothelial corneal dystrophy (Orphanet:98974)
Gelatinous drop-like corneal dystrophy (Orphanet:98957)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hurler syndrome (Orphanet:93473)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Isolated ectopia lentis (Orphanet:1885)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Lisch epithelial corneal dystrophy (Orphanet:98955)
Macular corneal dystrophy (Orphanet:98969)
Meesmann corneal dystrophy (Orphanet:98954)
Microcystic corneal dystrophy (Orphanet:98956)
Mucolipidosis type 2 (Orphanet:576)
Multiple endocrine neoplasia type 2 (Orphanet:653)
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 (OMIM:600462)
Neurofaciodigitorenal syndrome (Orphanet:2673)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Pachyonychia congenita (Orphanet:2309)
Peters anomaly (Orphanet:708)
Posterior amorphous corneal dystrophy (Orphanet:98971)
Posterior polymorphous corneal dystrophy (Orphanet:98973)
Reis-Bücklers corneal dystrophy (Orphanet:98961)
Robinow-like syndrome (Orphanet:3105)
Spastic ataxia - corneal dystrophy (Orphanet:2572)
Stern-Lubinsky-Durrie syndrome (Orphanet:3194)
Sturge-Weber syndrome (Orphanet:3205)
Subepithelial mucinous corneal dystrophy (Orphanet:98959)
Thiel-Behnke corneal dystrophy (Orphanet:98960)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Tyrosinemia type 2 (Orphanet:28378)
X-linked endothelial corneal dystrophy (Orphanet:293621)