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Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
4 OMIM references -
4 associated genes
157 connected diseases
No signs/symptoms info
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Desmoplastic small round cell tumor
46,XY partial gonadal dysgenesis
Denys-Drash syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Frasier syndrome
Meacham syndrome
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WAGR syndrome
Autoimmune lymphoproliferative syndrome
Gastrointestinal stromal tumor
B-cell chronic lymphocytic leukemia
Hepatocellular carcinoma, childhood-onset
Juvenile myelomonocytic leukemia
Amyotrophic lateral sclerosis
Dedifferentiated liposarcoma
Multiple endocrine neoplasia type 1
Well-differentiated liposarcoma
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
Isolated bone marrow mastocytosis
Lymphoadenopathic mastocytosis with eosinophilia
Nodular urticaria pigmentosa
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
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Adrenocortical carcinoma
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor B-cell acute lymphoblastic leukemia
T-cell immunodeficiency with epidermodysplasia verruciformis
Neutrophil immunodeficiency syndrome
Cree leukoencephalopathy
Ewing sarcoma
Extraskeletal Ewing sarcoma
Extraskeletal myxoid chondrosarcoma
Melanoma of soft part
X-linked lymphoproliferative disease
Autosomal dominant nonsyndromic intellectual deficit
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
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
Mucocutaneous venous malformations
Myeloid neoplasm associated with PDGFRB rearrangement
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Papillary or follicular thyroid carcinoma
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
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Costello syndrome
Linear nevus sebaceus syndrome
Phakomatosis pigmentokeratotica
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
17q11 microdeletion syndrome
Adult-onset distal myopathy due to VCP mutation
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Baraitser-Winter syndrome
Behavioral variant of frontotemporal dementia
Boomerang dysplasia
Carney-Stratakis syndrome
Cerebellar ataxia-deafness-narcolepsy syndrome
Cowden syndrome
Dyskeratosis congenita
Estrogen resistance syndrome
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Frontotemporal dementia with motor neuron disease
Hereditary pheochromocytoma-paraganglioma
Hereditary spherocytosis
Hoyeraal-Hreidarsson syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Juvenile amyotrophic lateral sclerosis
Large congenital melanocytic nevus
Lethal acantholytic epidermolysis bullosa
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Multiple endocrine neoplasia type 4
Myxoid / round cell liposarcoma
Naxos disease
Noonan syndrome
Progressive non-fluent aphasia
Pseudohypoaldosteronism type 2E
Retinopathy - anemia- central nervous system anomalies
Semantic dementia
Spastic paraplegia - Paget disease of bone
Spondylocarpotarsal synostosis
Weaver syndrome
Zollinger-Ellison syndrome
Familial isolated dilated cardiomyopathy
Renal coloboma syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
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
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Autoimmune lymphoproliferative syndrome with recurrent infections
Bladder exstrophy
EEC syndrome
FADD-related immunodeficiency
Intermittent hydrarthrosis
Juvenile rheumatoid factor-negative polyarthritis
Limb-mammary syndrome
Oculootodental syndrome
Oligoarticular juvenile arthritis
Split hand-split foot malformation
Squamous cell carcinoma of head and neck
TRAPS syndrome
(no synonyms)

Classification (Orphanet):
- Rare genetic disease
- Rare renal disease

Classification (ICD10):
- Diseases of the genitourinary system -

Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references

Gene symbol UniProt reference OMIM reference
ARHGDIA P52565601925
PLCE1 Q9P212608414
PTPRO Q16827600579
WT1 P19544607102
No signs/symptoms info available.