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Oligoarticular juvenile arthritis
9 associated genes
127 connected diseases
5 signs/symptoms
Disease Type of connection
Juvenile rheumatoid factor-negative polyarthritis
Pediatric systemic lupus erythematosus
T-B+ severe combined immunodeficiency due to CD3delta / CD3epsilon / CD3zeta
Autoimmune lymphoproliferative syndrome
Behçet disease
Giant cell arteritis
Granulomatosis with polyangiitis
Immunodeficiency due to CD25 deficiency
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Acute promyelocytic leukemia
Severe combined immunodeficiency due to LCK deficiency
Chronic mucocutaneous candidiasis
T-B+ severe combined immunodeficiency due to JAK3 deficiency
Autosomal dominant hyper-IgE syndrome
Laron syndrome with immunodeficiency
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Laron syndrome
Short stature due to partial GHR deficiency
Juvenile myelomonocytic leukemia
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Amyotrophic lateral sclerosis
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Idiopathic hypereosinophilic syndrome
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Combined immunodeficiency due to ZAP70 deficiency
Familial isolated dilated cardiomyopathy
Giant cell glioblastoma
Autosomal agammaglobulinemia
SHORT syndrome
FADD-related immunodeficiency
Oculootodental syndrome
Autoimmune lymphoproliferative syndrome with recurrent infections
Cone rod dystrophy
Idiopathic CD4 lymphocytopenia
Omenn syndrome
T-B+ severe combined immunodeficiency due to gamma chain deficiency
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Rabson-Mendenhall syndrome
Distal 22q11.2 microdeletion syndrome
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Spinocerebellar ataxia type 2
Catecholaminergic polymorphic ventricular tachycardia
Adult-onset distal myopathy due to VCP mutation
Autosomal recessive systemic lupus erythematosus
Behavioral variant of frontotemporal dementia
Common variable immunodeficiency
Familial medullary thyroid carcinoma
Hereditary cerebral cavernous malformation
Hereditary sensory and autonomic neuropathy type 4
Hereditary sensory and autonomic neuropathy type 5
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Papillary or follicular thyroid carcinoma
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Wiskott-Aldrich syndrome
X-linked severe congenital neutropenia
X-linked thrombocytopenia with normal platelets
Intellectual deficiency - hypotonia - spasticity - sleep disorder
Solitary fibrous tumor
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant centronuclear myopathy
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Autosomal recessive limb-girdle muscular dystrophy type 2G
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
Bladder exstrophy
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
EEC syndrome
Endocrine-cerebro-osteodysplasia syndrome
Fetal akinesia-cerebral and retinal hemorrhage syndrome
Hereditary spherocytosis
Hyperlipoproteinemia type 4
Hyperlipoproteinemia type 5
Intermediate nemaline myopathy
Limb-mammary syndrome
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
Muscular dystrophy, Selcen type
Reducing body myopathy
Severe congenital nemaline myopathy
Split hand-split foot malformation
Typical nemaline myopathy
X-linked Emery-Dreifuss muscular dystrophy
X-linked myopathy with postural muscle atrophy
Growth retardation-mild developmental delay-chronic hepatitis syndrome
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
Primary biliary cirrhosis
Herpetic encephalitis
T-B+ severe combined immunodeficiency due to CD45 deficiency
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial papillary renal cell carcinoma
Hepatocellular carcinoma, childhood-onset
Intermittent hydrarthrosis
Squamous cell carcinoma of head and neck
TRAPS syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Combined deficiency of factor V and factor VIII
LEOPARD syndrome
Noonan syndrome
Pilocytic astrocytoma
Precursor T-cell acute lymphoblastic leukemia
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Romano-Ward syndrome
- Pauciarticular chronic arthritis

Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
No MeSH references

Very frequent
- Articular / joint pain / arthralgia
- Autoimmunity / autoimmune reaction / autoantibodies
- Biological inflammatory syndrome / increased erythrocyte sedimentation rate / CRP
- Hydrarthrosis / articular / joint effusion

- Chronic uveitis / blepharitis / episcleritis / scleritis / conjonctivitis / keratitis