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Ontology Browser
Term:
familial nephrotic syndrome (DOID:2590)
Annotations: Rat: (48) Mouse: (49) Human: (54) Chinchilla: (45) Bonobo: (45) Dog: (45) Squirrel: (45) Pig: (46)
Parent Terms Term With Siblings Child Terms
monogenic disease +     
nephrotic syndrome +     
Alport syndrome +   
anterior segment dysgenesis +   
autosomal genetic disease +   
Bartter disease +   
basal laminar drusen  
Brugada syndrome +   
Camurati-Engelmann disease +   
cardiofaciocutaneous syndrome +   
cataract +   
catecholaminergic polymorphic ventricular tachycardia +   
chondrodysplasia punctata +   
Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome 
ciliopathy +   
cone-rod dystrophy +   
Cornelia de Lange syndrome +   
corticosteroid-binding globulin deficiency  
Cystinosis, Late-Onset Juvenile or Adolescent Nephropathic Type  
Diffuse Mesangial Sclerosis  
Diffuse Renal Mesangial Sclerosis, with Ocular Abnormalities 
dilated cardiomyopathy 1BB  
dilated cardiomyopathy 1EE  
dilated cardiomyopathy 1FF  
dilated cardiomyopathy 1G  
dilated cardiomyopathy 1GG  
dilated cardiomyopathy 1H  
dilated cardiomyopathy 1I  
dilated cardiomyopathy 1J  
dilated cardiomyopathy 1K 
dilated cardiomyopathy 1L  
dilated cardiomyopathy 1M  
dilated cardiomyopathy 1O  
dilated cardiomyopathy 1P  
dilated cardiomyopathy 1Q 
dilated cardiomyopathy 1T  
dilated cardiomyopathy 1W  
dilated cardiomyopathy 1Z  
erythrokeratodermia variabilis +   
familial hemophagocytic lymphohistiocytosis 5  
familial nephrotic syndrome +   
A nephrotic syndrome that has_material_basis_in genetic mutations. (DO)
Fanconi anemia complementation group F  
Fanconi anemia complementation group G  
Fanconi anemia complementation group J  
Fanconi anemia complementation group N  
Feigenbaum Bergeron Richardson Syndrome 
fetal akinesia deformation sequence syndrome +   
gene duplication disease +   
hereditary combined deficiency of vitamin K-dependent clotting factors +   
Hutterite Cerebroosteonephrodysplasia Syndrome 
hypochondrogenesis  
infantile histiocytoid cardiomyopathy  
inflammatory bowel disease 1  
inflammatory bowel disease 10  
inflammatory bowel disease 11 
inflammatory bowel disease 12  
inflammatory bowel disease 13  
inflammatory bowel disease 14  
inflammatory bowel disease 15 
inflammatory bowel disease 16  
inflammatory bowel disease 17  
inflammatory bowel disease 18 
inflammatory bowel disease 19  
inflammatory bowel disease 2 
inflammatory bowel disease 20 
inflammatory bowel disease 22 
inflammatory bowel disease 23 
inflammatory bowel disease 24 
inflammatory bowel disease 26 
inflammatory bowel disease 27 
inflammatory bowel disease 4 
inflammatory bowel disease 5  
inflammatory bowel disease 6 
inflammatory bowel disease 7 
inflammatory bowel disease 8 
inflammatory bowel disease 9 
isolated microphthalmia 4  
Junctional Epidermolysis Bullosa 7, with Interstitial Lung Disease and Nephrotic Syndrome  
lambda 5 deficiency 
Leber congenital amaurosis 10  
Leber congenital amaurosis 3  
Leber congenital amaurosis 7  
lipoid nephrosis  
multiple epiphyseal dysplasia due to collagen 9 anomaly +   
multiple pterygium syndrome +   
Nephrotic Syndrome with Ocular Anomalies 
Noonan syndrome +   
osteogenesis imperfecta type 14  
osteogenesis imperfecta type 6  
Pierson syndrome  
posterior polymorphous corneal dystrophy 3  
postural orthostatic tachycardia syndrome  
primary congenital glaucoma +   
Ritscher-Schinzel syndrome +   
Schimke immuno-osseous dysplasia  
schizophrenia 13 
schizophrenia 14 
schizophrenia 16  
schizophrenia 18  
schizophrenia 9  
SHOX-related short stature  
X-linked monogenic disease +   
Y-linked monogenic disease +   

Synonyms
Exact Synonyms: CNF ;   congenital nephrosis ;   congenital nephrotic syndrome ;   genetic nephrotic syndrome ;   hereditary nephrotic syndrome ;   hereditary nephrotic syndromes
Primary IDs: MESH:C535761
Xrefs: ICD10CM:N04 ;   NCI:C35337 ;   OMIM:PS256300 ;   ORDO:564127
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/19066979 "DO" "DO"

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