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Symbol
Name
ID
Ndp
Norrie disease (pseudoglioma) (human)
MGI:102570
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Vitreous hemorrhage
Deeply set eye
Hypotelorism
Microphthalmia
Abnormality of the retinal vasculature
Peripheral retinal avascularization
Retinal neovascularization
Retinal vascular tortuosity
Anterior chamber synechiae
Shallow anterior chamber
Opacification of the corneal stroma
Sclerocornea
Abnormal pupil morphology
Hypoplasia of the iris
Aplasia/Hypoplasia of the lens
Cataract
Subcapsular cataract
Ectopia lentis
Abnormal chorioretinal morphology
Retinal detachment
Tractional retinal detachment
Retinal dysplasia
Retinal fold
Falciform retinal fold
Retinal hole
Retinal exudate
Intraretinal exudate
Subretinal exudate
Optic atrophy
Peripheral vitreous opacities
Posterior vitreous detachment
Remnants of the hyaloid vascular system
Exudative vitreoretinopathy
Neoplasm of the eye
Nystagmus
Horizontal pendular nystagmus
Reduced visual acuity
Visual impairment
Blindness
Glaucoma
Disease(s) Associated with NDP
exudative vitreoretinopathy
Norrie disease

Mouse Phenotypes
vision/eye phenotype
abnormal retinal vasculature morphology
decreased retinal photoreceptor cell number
photoreceptor outer segment degeneration
abnormal retinal pigmentation
disorganized retinal ganglion layer
abnormal retinal inner nuclear layer morphology
abnormal retinal outer nuclear layer morphology
abnormal retinal outer plexiform layer morphology
abnormal retinal photoreceptor layer morphology
disorganized retinal layers
abnormal vitreous body morphology
vitreous body deposition
Availability Mouse Genotype
Ndptm1Lex/Ndptm1Lex
Ndptm1Wbrg/Ndp+ *
Ndptm2Nat/Ndp+
Ndptm1Lex/Y
Ndptm1Wbrg/Y

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/12/2019
MGI 6.13
The Jackson Laboratory