Vitreous hemorrhage

Symptom Information:

Symptom ID: HPO:0007902
Synonyms:
Vitreous haemorrhage [HPO:0007902]
Vitreous hemorrhage [OMIM:Vitreous hemorrhage]
Vitreous hemorrhage (rare) [OMIM:Vitreous hemorrhage (rare)]
Vitreous haemorrhage [MedDRA:10047655]
Quality:
Cross references:
OMIM: "Vitreous hemorrhage" [OMIM:Vitreous hemorrhage]
OMIM: "Vitreous hemorrhage (rare)" [OMIM:Vitreous hemorrhage (rare)]
Is a (Direct Parents):
MedDRA Ocular haemorrhagic disorders
HPO         Abnormality of the vitreous humor
HPO         Hemorrhage of the eye
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormal bleeding(HPO:0001892)
             Internal hemorrhage(HPO:0011029)
                Hemorrhage of the eye(HPO:0011885)
                   Vitreous hemorrhage(HPO:0007902)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the vitreous humor(HPO:0004327)
                      Vitreous hemorrhage(HPO:0007902)
          Abnormal eye physiology(HPO:0012373)
             Hemorrhage of the eye(HPO:0011885)
                Vitreous hemorrhage(HPO:0007902)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of cardiovascular system physiology(HPO:0011025)
             Abnormality of blood circulation(HPO:0011028)
                Internal hemorrhage(HPO:0011029)
                   Hemorrhage of the eye(HPO:0011885)
                      Vitreous hemorrhage(HPO:0007902)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular haemorrhagic disorders(MedDRA:10047075)
       Ocular haemorrhagic disorders(MedDRA:10064464)
          Vitreous hemorrhage(HPO:0007902)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant neovascular inflammatory vitreoretinopathy (Orphanet:329211)
EXUDATIVE VITREORETINOPATHY 4 (OMIM:601813)
Familial exudative vitreoretinopathy (Orphanet:891)
Insulin-resistance syndrome type A (Orphanet:2297)
MRCS syndrome (Orphanet:263347)
RETINAL VENOUS BEADING (OMIM:180080)
Retinoblastoma (Orphanet:790)
Retinopathy of prematurity (Orphanet:90050)
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE (OMIM:612304)