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Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
1 OMIM reference -
2 associated genes
73 connected diseases
No signs/symptoms info
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Congenital nephrotic syndrome, Finnish type
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Hepatocellular carcinoma, childhood-onset
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
X-linked intellectual deficit, Najm type
EEM syndrome
Hypotrichosis with juvenile macular degeneration
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Cutaneous mastocytoma
Gastrointestinal stromal tumor
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Nodular urticaria pigmentosa
Piebaldism
Plaque-form urticaria pigmentosa
Pseudoxanthomatous diffuse cutaneous mastocytosis
Smouldering systemic mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Congenital analbuminemia
Autosomal dominant nonsyndromic intellectual deficit
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Craniopharyngioma
Desmoid tumor
Familial medullary thyroid carcinoma
Familial papillary renal cell carcinoma
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Hyperinsulinism due to INSR deficiency
Idiopathic hypereosinophilic syndrome
Infantile myofibromatosis
Insulin-resistance syndrome type A
Juvenile myelomonocytic leukemia
Leprechaunism
Mucocutaneous venous malformations
Myeloid neoplasm associated with PDGFRB rearrangement
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Papillary or follicular thyroid carcinoma
Pilomatrixoma
Primary familial polycythemia
Rabson-Mendenhall syndrome
Severe combined immunodeficiency due to LCK deficiency
Unclassified chronic myeloproliferative disease
Wiskott-Aldrich syndrome
X-linked severe congenital neutropenia
X-linked thrombocytopenia with normal platelets
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Baraitser-Winter syndrome
Behavioral variant of frontotemporal dementia
Hereditary spherocytosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the genitourinary system -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
NPHS1 O60500602716
PTPRO Q16827600579
No signs/symptoms info available.