Remnants of the hyaloid vascular system

Symptom Information:

Symptom ID: HPO:0007968
Synonyms:
Persistent hyperplasia of primary vitreous [HPO:0007968]
Persistent hypertrophic primary vitreous [HPO:0007968]
Persistent hyaloid artery (disorder) [Orphanet:5000]
Persistent primary vitreous (disorder) [Orphanet:5000]
Persistent hyperplastic primary vitreous (disorder) [Orphanet:5000]
Persistent Hyperplastic Primary Vitreous [Orphanet:5000]
Persistent primary vitreous [Orphanet:5000]
Persistent hyperplasia of primary vitreous [OMIM:Persistent hyperplasia of primary vitreous]
Persistent hyperplastic primary vitreous [OMIM:Persistent hyperplastic primary vitreous]
Vitreous anomalies/hyalitis/persistent vitreous vascularisation [Orphanet:5000]
Persistent hypertrophic primary vitreous (PHPV) [OMIM:Persistent hypertrophic primary vitreous (PHPV)]
Persistent primary vitreous [OMIM:Persistent primary vitreous]
Quality:
Cross references:
Orphanet:5000 "Vitreous anomalies/hyalitis/persistent vitreous vascularisation" [Orphanet:5000]
OMIM: "Persistent hyperplasia of primary vitreous" [OMIM:Persistent hyperplasia of primary vitreous]
OMIM: "Persistent hyperplastic primary vitreous" [OMIM:Persistent hyperplastic primary vitreous]
OMIM: "Persistent hypertrophic primary vitreous (PHPV)" [OMIM:Persistent hypertrophic primary vitreous (PHPV)]
OMIM: "Persistent primary vitreous" [OMIM:Persistent primary vitreous]
UMLS:C0266568 "Persistent Hyperplastic Primary Vitreous" [Orphanet:5000]
UMLS:C0266559 "Persistent primary vitreous" [Orphanet:5000]
Is a (Direct Parents):
Orphanet Abnormality of the vitreous humor
Orphanet Abnormality of the eye
HPO         Abnormality of the vitreous humor
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)
                      Remnants of the hyaloid vascular system(HPO:0007968)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Congenital blindness due to retinal non-attachment (Orphanet:300337)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Oculofaciocardiodental syndrome (Orphanet:2712)
REESE RETINAL DYSPLASIA (OMIM:266400)