modern wellness · Symptom
Corneal dystrophy
🩺 HPO Source
HPO ID
HPO Label
Corneal dystrophy
HPO Definition
The term corneal dystrophy embraces a heterogenous group of bilateral genetically determined non-inflammatory corneal diseases that are restricted to the cornea.
🔗 Cross-References (2)
SNOMEDCT_US5587004
UMLSC0010036
🔼 Broader Terms (1)
HP:0000481Abnormal cornea morphology
🏥 Conditions where Corneal dystrophy appears
23 · bridged via HPO ↔ OMIM
syndrome OMIM 217400
Corneal Dystrophy And Perceptive Deafness
ev: IEA
syndrome OMIM 610048
Corneal Dystrophy, Congenital Stromal
freq: 11/11 onset: HP:0003623 ev: PCS
syndrome OMIM 121820
Corneal Dystrophy, Epithelial Basement Membrane
ev: PCS
syndrome OMIM 610158
Corneal Dystrophy, Fuchs Endothelial, 2
ev: IEA
syndrome OMIM 613268
Corneal Dystrophy, Fuchs Endothelial, 4
ev: PCS
syndrome OMIM 613270
Corneal Dystrophy, Fuchs Endothelial, 6
ev: IEA
syndrome OMIM 615523
Corneal Dystrophy, Fuchs Endothelial, 8
ev: PCS
syndrome OMIM 136800
Corneal Dystrophy, Fuchs' Endothelial, 1
ev: TAS
disease OMIM 122100
Corneal Dystrophy, Juvenile Epithelial of Meesmann
ev: PCS
syndrome OMIM 204870
Corneal Dystrophy, Lattice Type 3
onset: HP:0011463 ev: PCS
syndrome OMIM 612868
Corneal Dystrophy, Posterior Amorphous
ev: IEA
syndrome OMIM 609140
Corneal Dystrophy, Posterior Polymorphous, 2
ev: TAS
syndrome OMIM 609141
Corneal Dystrophy, Posterior Polymorphous, 3 (Disorder)
freq: 11/11 ev: PCS
syndrome OMIM 217700
Corneal Endothelial Dystrophy 2
onset: HP:0003577 ev: PCS
syndrome OMIM 301500
Fabry Disease
ev: IEA
syndrome OMIM 301500
Fabry Disease, Cardiac Variant
ev: IEA
syndrome OMIM 308800
Keratosis Follicularis Spinulosa Decalvans, X-Linked
ev: IEA
syndrome OMIM 217800
Macular Dystrophy, Corneal Type 1
ev: IEA
syndrome OMIM 253250
Mulibrey Nanism
freq: 4/42 ev: PCS
syndrome OMIM 608470
Reis-Bucklers' Corneal Dystrophy
freq: 9/9 ev: PCS
syndrome OMIM 121800
Schnyder Crystalline Corneal Dystrophy
ev: IEA
syndrome OMIM 617763
Short Stature, Hearing Loss, Retinitis Pigmentosa, And Distinctive Facies
freq: 1/3 ev: PCS
syndrome OMIM 602082
Thiel-Behnke Corneal Dystrophy
ev: IEA