MGI 5.13 - Phenotype Browser

Mammalian Phenotype Browser
Term Detail

MP term:	persistence of hyaloid vascular system
Synonym:	persistence of hyaloid capillary system
MP id:	MP:0001289
Definition:	failure of the degeneration of the transient vascular system of the eye during development, that normally nourishes the retina, immature lens and primary vitreous of the developing eye
Number of paths to term:	2

denotes an 'is-a' relationship
denotes a 'part-of' relationship

mammalian phenotype

vision/eye phenotype

abnormal eye morphology

abnormal eye development

abnormal corneal stroma development

abnormal eye muscle development

abnormal eyelid development +

abnormal lens development +

abnormal optic cup morphology

abnormal optic eminence morphology

abnormal optic stalk morphology

abnormal optic vesicle formation +

abnormal periocular mesenchyme morphology

abnormal primary vitreous morphology +

abnormal retinal development +

aniridia

coloboma +

cyclopia

ectopia lentis

eye bleb

lenticonus

mammalian phenotype

vision/eye phenotype

abnormal eye morphology

abnormal posterior eye segment morphology

abnormal vitreous body morphology

abnormal primary vitreous morphology +

opacity of vitreous body

persistence of hyaloid vascular system [MP:0001289] (32 genotypes, 32 annotations)

vitreal fibroplasia

vitreous body deposition

vitreous body hemorrhage

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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