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Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
11 OMIM references -
12 associated genes
234 connected diseases
No signs/symptoms info
Disease Type of connection
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Congenital nephrotic syndrome, Finnish type
Sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Sporadic idiopathic steroid-resistant nephrotic syndrome with minimal changes
46,XY partial gonadal dysgenesis
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Denys-Drash syndrome
Desmoplastic small round cell tumor
Frasier syndrome
Meacham syndrome
Nephroblastoma
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WAGR syndrome
Juvenile myelomonocytic leukemia
Familial isolated dilated cardiomyopathy
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Noonan syndrome
Left ventricular noncompaction
Precursor B-cell acute lymphoblastic leukemia
Hepatocellular carcinoma, childhood-onset
Autosomal dominant nonsyndromic intellectual deficit
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Familial pancreatic carcinoma
X-linked intellectual deficit, Najm type
EEM syndrome
Hypotrichosis with juvenile macular degeneration
B-cell chronic lymphocytic leukemia
Giant cell glioblastoma
Gliosarcoma
Craniopharyngioma
Desmoid tumor
Pilomatrixoma
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant centronuclear myopathy
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Papillary or follicular thyroid carcinoma
Precursor T-cell acute lymphoblastic leukemia
Autosomal agammaglobulinemia
Atrial septal defect, ostium secundum type
Chronic mucocutaneous candidiasis
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Acute myeloblastic leukemia with maturation
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
Baraitser-Winter syndrome
Autoimmune lymphoproliferative syndrome
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Early-onset autosomal dominant Alzheimer disease
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
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
Large congenital melanocytic nevus
Acute encephalopathy with biphasic seizures and late reduced diffusion
Adrenocortical carcinoma
Essential thrombocythemia
Generalized junctional epidermolysis bullosa, non-Herlitz type
Late-onset junctional epidermolysis bullosa
Li-Fraumeni syndrome
Localized junctional epidermolysis bullosa, non-Herlitz type
Papilloma of choroid plexus
Familial amyloidosis, Finnish type
Autosomal dominant macrothrombocytopenia
Chronic intestinal pseudoobstruction
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Estrogen resistance syndrome
Frontometaphyseal dysplasia
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Terminal osseous dysplasia - pigmentary defects
Familial gastric cancer
Gastric linitis plastica
Congenital analbuminemia
Fibronectin glomerulopathy
Spinocerebellar ataxia type 15 / 16
Spinocerebellar ataxia type 29
Atypical juvenile parkinsonism
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Familial medullary thyroid carcinoma
Familial melanoma
Familial papillary renal cell carcinoma
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Hyperinsulinism due to INSR deficiency
Hypocalcemic vitamin D-resistant rickets
Idiopathic hypereosinophilic syndrome
Infantile myofibromatosis
Insulin-resistance syndrome type A
Leprechaunism
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Mucocutaneous venous malformations
Myeloid neoplasm associated with PDGFRB rearrangement
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
Congenital plasminogen activator inhibitor type 1 deficiency
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
17p13.3 microduplication syndrome
17q11 microdeletion syndrome
3C syndrome
AICA-ribosiduria
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Autosomal dominant slowed nerve conduction velocity
Autosomal dominant spastic paraplegia type 8
Autosomal recessive centronuclear myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2J
Autosomal recessive nonsyndromic intellectual deficit
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Boomerang dysplasia
Cerebellar ataxia-deafness-narcolepsy syndrome
Chronic myeloid leukemia
Common variable immunodeficiency
Congenital microcephaly-severe encephalopathy-progressive cerebral atrophy syndrome
Craniometaphyseal dysplasia
Distal myopathy with posterior leg and anterior hand involvement
Early-onset myopathy with fatal cardiomyopathy
Familial dysautonomia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Glucocorticoid resistance
Hereditary proximal myopathy with early respiratory failure
Hereditary spherocytosis
Huntington disease
Hypoplastic left heart syndrome
Intellectual deficit, X-linked, Turner type
Jeune syndrome
Juvenile Huntington disease
Lissencephaly due to LIS1 mutation
Meckel syndrome
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Microcephalic primordial dwarfism, Alazami type
Miller-Dieker syndrome
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
Multiple endocrine neoplasia type 1
Muscle filaminopathy
Oculodentodigital dysplasia
Spinocerebellar ataxia type 7
Spondylocarpotarsal synostosis
Spondylometaphyseal dysplasia - cone-rod dystrophy
Subcortical band heterotopia
Susceptibility to viral and mycobacterial infections
Syndactyly type 3
Tibial muscular dystrophy
Weaver syndrome
X-linked Emery-Dreifuss muscular dystrophy
Zollinger-Ellison syndrome
Autosomal recessive distal renal tubular acidosis with deafness
Childhood-onset nemaline myopathy
Intermediate nemaline myopathy
Renal coloboma syndrome
Severe congenital nemaline myopathy
Typical nemaline myopathy
Developmental malformations - deafness - dystonia
Hereditary gingival fibromatosis
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Bladder exstrophy
Combined immunodeficiency due to ORAI1 deficiency
EEC syndrome
LEOPARD syndrome
Limb-mammary syndrome
Metachondromatosis
Pyogenic arthritis - pyoderma gangrenosum - acne
Split hand-split foot malformation
SHORT syndrome
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Charcot-Marie-Tooth disease type 2B1
Congenital muscular dystrophy due to LMNA mutation
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Familial aortic dissection
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Familial thoracic aortic aneurysm and aortic dissection
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
Synonym(s):
- Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis

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

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

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
11 OMIM references -
No MeSH references

No signs/symptoms info available.