Corneal dystrophy
Symptom Information:
Symptom ID: | HPO:0001131 | ||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||||
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) |