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Ontology Browser

Term:
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities (DOID:9007459)
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Parent Terms Term With Siblings Child Terms
Eye Abnormalities +     
nephrotic syndrome +     
Sclerosis +     
3MC syndrome 1  
ablepharon macrostomia syndrome  
aniridia +   
Ankyloblepharon Filiforme Adnatum 
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome  
Anophthalmia +   
anterior segment dysgenesis +   
Asymmetric Short Stature Syndrome 
Axenfeld-Rieger syndrome +   
Basel-Vanagaite-Smirin-Yosef syndrome  
blepharophimosis +   
Blue Diaper Syndrome 
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism 
Brittle Cornea Syndrome +   
Chemke Oliver Mallek Syndrome 
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
Choroidal Effusions +  
chromosome 6pter-p24 deletion syndrome 
CODAS syndrome  
Cole-Carpenter syndrome +   
coloboma +   
Colobomatous Macrophthalmia with Microcornea 
Congenital Nephrotic Syndrome with or without Ocular Abnormalities +   
Craniofacial Anomalies and Anterior Segment Dysgenesis Syndrome  
Craniosynostosis with Ocular Abnormalities and Hallucal Defects 
cryptophthalmia +   
Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type  
De Hauwere syndrome 
Desanto-Shinawi Syndrome  
Diffuse Mesangial Sclerosis  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
Dwarfism Stiff Joint Ocular Abnormalities 
Ectopia Lentis +   
Egg-Shaped Pupil 
exudative vitreoretinopathy +   
FACES Syndrome 
familial nephrotic syndrome +   
Feigenbaum Bergeron Richardson Syndrome 
Foveal Hypoplasia and Anterior Segment Dysgenesis  
Fronto-Facio-Nasal Dysplasia 
Frontoocular Syndrome 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Hereditary Sclerosing Poikiloderma +   
Hutterite Cerebroosteonephrodysplasia Syndrome 
hydrophthalmos +   
Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital  
iridogoniodysgenesis syndrome +   
Joubert syndrome 1  
Joubert Syndrome 2  
Joubert syndrome 9  
Kapur Toriello Syndrome 
lipoid nephrosis  
Maxillofacial Dysostosis 
Mediastinal Fibrosis 
Microcornea, Glaucoma, and Absent Frontal Sinuses 
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
microphthalmia +   
MOMES Syndrome 
Nephrotic Syndrome with Ocular Anomalies 
Neurodevelopmental Disorder with or without Anomalies of the Brain, Eye, or Heart  
oblique facial clefting 1  
oculoauricular syndrome  
Oculoauriculofrontonasal Syndrome 
Oculocerebrocutaneous Syndrome 
oculodentodigital dysplasia +   
Oculopalatocerebral Syndrome 
Oculorenocerebellar Syndrome 
Osteosclerosis with Ichthyosis and Premature Ovarian Failure 
Pena Shokeir Syndrome Type 2 
persistent hyperplastic primary vitreous +   
PHACE Association  
Pierson syndrome  
popliteal pterygium syndrome +   
Prepapillary Vascular Loops 
Pupillary Membrane, Persistence of 
Retinal Dysplasia +   
Rozin Hertz Goodman Syndrome 
Schimke immuno-osseous dysplasia  
Schmid-Fraccaro Syndrome  
Sclerosing Bone Dysplasia, Mental Retardation 
Sclerosing Lymphocytic Lobulitis 
Stromme syndrome  
torsion dystonia with onset in infancy  
Ullrich congenital muscular dystrophy +   

Synonyms
Primary IDs: MESH:C565405 ;   RDO:0014049

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