Coloboma of eye lens |
98943 |
A rare, genetic, developmental defect… |
Orphanet, ICD-10 |
Coloboma of iris |
98944 |
A rare, genetic, developmental defect… |
Orphanet, OMIM, MedDRA, ICD-10 |
Coloboma of macula |
98945 |
Coloboma of macula is a rare, non-… |
Orphanet, ICD-10 |
Coloboma of eyelid |
98946 |
A rare, genetic, developmental defect… |
Orphanet, ICD-10 |
Coloboma of optic disc |
98947 |
Coloboma of optic disc is a rare,… |
Orphanet, ICD-10 |
Complete cryptophthalmia |
98949 |
|
Orphanet, ICD-10, OMIM |
Meesmann corneal dystrophy |
98954 |
Meesmann corneal dystrophy (MECD) is a… |
Orphanet, OMIM, MeSH, ICD-10, OMIM |
Epithelial basement membrane dystrophy |
98956 |
A rare corneal dystrophy characterized… |
Orphanet, ICD-10, OMIM |
Gelatinous drop-like corneal dystrophy |
98957 |
Gelatinous drop-like corneal dystrophy… |
Orphanet, MeSH, OMIM, ICD-10 |
Thiel-Behnke corneal dystrophy |
98960 |
Thiel-Behnke corneal dystrophy (TBCD)… |
Orphanet, ICD-10, MeSH, OMIM |
Reis-Bücklers corneal dystrophy |
98961 |
Reis-Bücklers corneal dystrophy (RBCD… |
Orphanet, MeSH, ICD-10, OMIM |
Granular corneal dystrophy type I |
98962 |
Type I granular corneal dystrophy (GCDI… |
Orphanet, OMIM, ICD-10 |
Granular corneal dystrophy type II |
98963 |
Type II granular corneal dystrophy (… |
Orphanet, MeSH, OMIM, ICD-10 |
Lattice corneal dystrophy type I |
98964 |
Type I lattice corneal dystrophy (LCDI… |
Orphanet, ICD-10, OMIM, OMIM, MeSH |
Schnyder corneal dystrophy |
98967 |
Schnyder corneal dystrophy (SCD) is a… |
Orphanet, MeSH, ICD-10, OMIM |
Macular corneal dystrophy |
98969 |
Macular corneal dystrophy (MCD) is a… |
Orphanet, OMIM, MedDRA, ICD-10 |
Fleck corneal dystrophy |
98970 |
Fleck corneal dystrophy (FCD) is a rare… |
Orphanet, OMIM, ICD-10 |
Posterior polymorphous corneal dystrophy |
98973 |
A rare mild subtype of posterior… |
Orphanet, OMIM, OMIM, ICD-10, OMIM |
Fuchs endothelial corneal dystrophy |
98974 |
A disorder that is the most frequent… |
Orphanet, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, OMIM, ICD-10 |
Congenital hereditary endothelial dystrophy type I |
98975 |
A rare subtype of posterior corneal… |
Orphanet, OMIM, ICD-10 |