Keratoconus

Symptom Information:

Symptom ID: HPO:0000563
Synonyms:
Keratoconus (disorder) [Orphanet:4480]
Keratoconus [Orphanet:4480]
Keratoconus [OMIM:Keratoconus]
Keratoconus/keratoglobus [Orphanet:4480]
Keratoconus [MedDRA:10023353]
Keratoconus, acute hydrops [MedDRA:10023353]
Keratoconus, stable condition [MedDRA:10023353]
Keratoconus, unspecified [MedDRA:10023353]
Keratoconus (in some patients) [OMIM:Keratoconus (in some patients)]
Keratoconus (less common) [OMIM:Keratoconus (less common)]
Quality:
Cross references:
Orphanet:4480 "Keratoconus/keratoglobus" [Orphanet:4480]
OMIM: "Keratoconus" [OMIM:Keratoconus]
OMIM: "Keratoconus (in some patients)" [OMIM:Keratoconus (in some patients)]
OMIM: "Keratoconus (less common)" [OMIM:Keratoconus (less common)]
UMLS:C0022578 "Keratoconus" [HPO:0000563]
UMLS:C0022578 "Keratoconus" [Orphanet:4480]
Is a (Direct Parents):
HPO         Increased corneal curvature
HPO         Decreased corneal thickness
MedDRA Corneal structural change, deposit and degeneration
Orphanet Abnormality of the eye
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)
                      Abnormality of the curvature of the cornea(HPO:0100691)
                         Increased corneal curvature(HPO:0100692)
                            Keratoconus(HPO:0000563)
                      Abnormality of corneal thickness(HPO:0011486)
                         Decreased corneal thickness(HPO:0100689)
                            Keratoconus(HPO:0000563)
MedDRA:
Eye disorders(MedDRA:10015919)
    Anterior eye structural change, deposit and degeneration(MedDRA:10002693)
       Corneal structural change, deposit and degeneration(MedDRA:10011049)
          Keratoconus(HPO:0000563)
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
BRITTLE CORNEA SYNDROME 1 (OMIM:229200)
BRITTLE CORNEA SYNDROME 2 (OMIM:614170)
Brittle cornea syndrome (Orphanet:90354)
DERMATITIS, ATOPIC (OMIM:603165)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
GAPO syndrome (Orphanet:2067)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
KERATOCONUS 1 (OMIM:148300)
KERATOCONUS 5 (OMIM:614622)
KERATOCONUS 6 (OMIM:614623)
KERATOCONUS 7 (OMIM:614629)
KERATOCONUS 8 (OMIM:614628)
KERATOCONUS POSTICUS CIRCUMSCRIPTUS (OMIM:244600)
Leber congenital amaurosis 1 (OMIM:204000)
Leber congenital amaurosis 10 (OMIM:611755)
Leber congenital amaurosis 2 (OMIM:204100)
Leber congenital amaurosis 4 (OMIM:604393)
Leber congenital amaurosis 6 (OMIM:613826)
Leber congenital amaurosis 7 (OMIM:613829)
Leber congenital amaurosis 8 (OMIM:613835)
MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK (OMIM:609438)
Nail-patella syndrome (Orphanet:2614)