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Inflammatory myofibroblastic tumor
6 associated genes
221 connected diseases
No signs/symptoms info
Disease Type of connection
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Cap myopathy
Intermediate nemaline myopathy
Translocation renal cell carcinoma
ALK-positive anaplastic large cell lymphoma
ALK-positive large B-cell lymphoma
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Young adult-onset Parkinsonism
Precursor T-cell acute lymphoblastic leukemia
Familial isolated dilated cardiomyopathy
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Left ventricular noncompaction
Cornelia de Lange syndrome
Acute myeloblastic leukemia with maturation
Hypohidrotic ectodermal dysplasia with immunodeficiency
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Autosomal dominant nonsyndromic intellectual deficit
Acute promyelocytic leukemia
Typical nemaline myopathy
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Atypical juvenile parkinsonism
Desmoid tumor
Fibronectin glomerulopathy
Wilson-Turner syndrome
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Cowden syndrome
Proteus syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Blue cone monochromatism
Cone rod dystrophy
Familial prostate cancer
Papillary or follicular thyroid carcinoma
Pseudohypoaldosteronism type 2E
Familial thoracic aortic aneurysm and aortic dissection
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Distal 22q11.2 microdeletion syndrome
Essential thrombocythemia
Familial pancreatic carcinoma
Giant cell glioblastoma
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Precursor B-cell acute lymphoblastic leukemia
Digitotalar dysmorphism
Sheldon-Hall syndrome
Trismus - pseudocamptodactyly
Dent disease type 2
Oculocerebrorenal syndrome
Huntington disease
Juvenile Huntington disease
T-B+ severe combined immunodeficiency due to JAK3 deficiency
APC-related attenuated familial adenomatous polyposis
Familial adenomatous polyposis due to 5q22.2 microdeletion
Gardner syndrome
Turcot syndrome with polyposis
Microcephaly-capillary malformation syndrome
Estrogen resistance syndrome
Alveolar soft-part sarcoma
Homozygous familial hypercholesterolemia
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Charcot-Marie-Tooth disease type 4D
Classic mast cell leukemia
Cutaneous mastocytoma
Gastrointestinal stromal tumor
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
Acute basophilic leukemia
Anaplastic ependymoma
Autosomal recessive spastic paraplegia type 20
Burkitt lymphoma
Common variable immunodeficiency
Congenital analbuminemia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Hyperparathyroidism - jaw tumor syndrome
Intermittent hydrarthrosis
Parathyroid carcinoma
TRAPS syndrome
Ewing sarcoma
Extraskeletal Ewing sarcoma
Peripheral primitive neuroectodermal tumor
Congenital myopathy with excess of thin filaments
Severe congenital nemaline myopathy
17q11 microdeletion syndrome
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Acute myeloid leukemia with CEBPA somatic mutations
Amyotrophic lateral sclerosis
Autoimmune polyendocrinopathy type 1
Autosomal agammaglobulinemia
Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant hyper-IgE syndrome
Autosomal dominant spastic paraplegia type 13
Autosomal recessive centronuclear myopathy
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
Budd-Chiari syndrome
Congenital bilateral absence of vas deferens
Congenital myasthenic syndromes with glycosylation defect
Craniolenticulosutural dysplasia
Craniometaphyseal dysplasia
Cystic fibrosis
Distal hereditary motor neuropathy type 5
Familial thrombocytosis
Hepatocellular carcinoma, childhood-onset
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary chronic pancreatitis
Hereditary sensory and autonomic neuropathy type 2
Hereditary site-specific ovarian cancer syndrome
Hypoplastic left heart syndrome
Hypotrichosis simplex of the scalp
Idiopathic bronchiectasis
Inherited acute myeloid leukemia
Jeune syndrome
Lethal encephalopathy due to mitochondrial and peroxisomal fission defect
MODY syndrome
Male infertility with normal virilization due to meiosis defect
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Muscular dystrophy, Selcen type
Myelofibrosis with myeloid metaplasia
Oculodentodigital dysplasia
Parkinsonian-pyramidal syndrome
Partial pancreatic agenesis
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Permanent neonatal diabetes mellitus
Polycythemia vera
Posterior polar cataract
Primary peritoneal carcinoma
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
Pseudohypoaldosteronism type 2C
Pyogenic arthritis - pyoderma gangrenosum - acne
Rare isolated myopia
Retinitis pigmentosa
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
SHORT syndrome
Saldino-Mainzer syndrome
Syndactyly type 3
Total congenital cataract
Woolly hair
X-linked dystonia-parkinsonism
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Aneurysm - osteoarthritis syndrome
2q37 microdeletion syndrome
Catecholaminergic polymorphic ventricular tachycardia
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
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Branchio-oculo-facial syndrome
Chronic myeloid leukemia
Familial infantile bilateral striatal necrosis
Hermansky-Pudlak syndrome with neutropenia
Li-Fraumeni syndrome
Papilloma of choroid plexus
Atypical Werner syndrome
Autosomal codominant severe lipodystrophic laminopathy
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal recessive Emery-Dreifuss muscular dystrophy
Capillary malformation - arteriovenous malformation
Charcot-Marie-Tooth disease type 2B1
Chronic intestinal pseudoobstruction
Congenital muscular dystrophy due to LMNA mutation
Congenital short bowel syndrome
Congenital valvular dysplasia
Dilated cardiomyopathy - hypergonadotropic hypogonadism
Distal hereditary motor neuropathy type 2
Distal myopathy with vocal cord weakness
Ehlers-Danlos syndrome with periventricular heterotopia
Encephalopathy due to hydroxykynureninuria
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
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 congenital asplenia
Familial partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Frontometaphyseal dysplasia
Glucocorticoid resistance
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
Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
Neuralgic amyotrophy
Osteodysplasty, Melnick-Needles type
Osteogenesis imperfecta type 3
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Parkes Weber syndrome
Periventricular nodular heterotopia
Progeria-associated arthropathy
Severe combined immunodeficiency due to DNA-PKcs deficiency
Terminal osseous dysplasia - pigmentary defects
(no synonyms)

Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
(no data available)

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

No signs/symptoms info available.