Keratoglobus

Symptom Information:

Symptom ID: HPO:0001119
Synonyms:
Congenital keratoglobus (disorder) [Orphanet:4480]
Keratoglobus [OMIM:Keratoglobus]
Keratoconus/keratoglobus [Orphanet:4480]
Quality:
Cross references:
Orphanet:4480 "Keratoconus/keratoglobus" [Orphanet:4480]
OMIM: "Keratoglobus" [OMIM:Keratoglobus]
UMLS:C0344530 "Keratoglobus" [HPO:0001119]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Increased corneal curvature
HPO         Decreased corneal thickness
Orphanet Keratoconus
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 corneal thickness(HPO:0011486)
                         Decreased corneal thickness(HPO:0100689)
                            Keratoglobus(HPO:0001119)
                      Abnormality of the curvature of the cornea(HPO:0100691)
                         Increased corneal curvature(HPO:0100692)
                            Keratoglobus(HPO:0001119)
MedDRA:
Database Frequency: 4 / 7739
Resource:

All diseases associated with this symptom:

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)