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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
+
Congenital Nephrotic Syndrome with or without Ocular Abnormalities
+
nephrotic syndrome type 1
nephrotic syndrome type 10
nephrotic syndrome type 11
nephrotic syndrome type 12
nephrotic syndrome type 13
nephrotic syndrome type 14
nephrotic syndrome type 15
nephrotic syndrome type 16
nephrotic syndrome type 17
nephrotic syndrome type 18
nephrotic syndrome type 19
nephrotic syndrome type 2
nephrotic syndrome type 20
nephrotic syndrome type 21
nephrotic syndrome type 22
nephrotic syndrome type 23
Nephrotic Syndrome Type 24
nephrotic syndrome type 3
nephrotic syndrome type 4
nephrotic syndrome type 5
nephrotic syndrome type 6
nephrotic syndrome type 7
nephrotic syndrome type 8
nephrotic syndrome type 9
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"