Abnormality of the vitreous humor

Symptom Information:

Symptom ID: HPO:0004327
Synonyms:
Vitreous anomaly [Orphanet:5000]
Vitreous anomalies [Orphanet:5000]
Vitreous anomalies/hyalitis/persistent vitreous vascularisation [Orphanet:5000]
Congenital vitreous anomaly [Orphanet:5000]
Congenital vitreous anomaly [MedDRA:10061085]
Congenital vitreous anomaly NOS [MedDRA:10061085]
Vitreous anomalies, congenital [MedDRA:10061085]
Quality:
Cross references:
Orphanet:5000 "Vitreous anomalies/hyalitis/persistent vitreous vascularisation" [Orphanet:5000]
UMLS:C0158564 "Vitreous anomalies" [Orphanet:5000]
Is a (Direct Parents):
HPO         Asteroid hyalosis
HPO         Abnormality of the posterior segment of the globe
Orphanet Abnormality of the eye
HPO         Optically empty vitreous
MedDRA Congenital posterior segment disorders (incl optic nerve)
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 posterior segment of the globe(HPO:0004329)
                   Abnormality of the vitreous humor(HPO:0004327)
MedDRA:
Eye disorders(MedDRA:10015919)
    Congenital eye disorders (excl glaucoma)(MedDRA:10010463)
       Congenital posterior segment disorders (incl optic nerve)(MedDRA:10010595)
          Abnormality of the vitreous humor(HPO:0004327)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Autosomal dominant rhegmatogenous retinal detachment (Orphanet:209867)
Autosomal recessive Stickler syndrome (Orphanet:250984)
Kniest dysplasia (Orphanet:485)
Knobloch syndrome (Orphanet:1571)
Marshall syndrome (Orphanet:560)
Microcornea - posterior megalolenticonus - persistent fetal vasculature - coloboma (Orphanet:231736)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Norrie disease (Orphanet:649)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 1 (Orphanet:90653)
Stickler syndrome type 2 (Orphanet:90654)
Walker-Warburg syndrome (Orphanet:899)