Abnormality of the vitreous humor
Symptom Information:
Symptom ID: | HPO:0004327 | |||||||
Synonyms: |
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Is a (Direct Parents): | ||||||||
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) |
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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) |