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Translocation renal cell carcinoma
1 OMIM reference -
7 associated genes
220 connected diseases
No signs/symptoms info
Disease Type of connection
Alveolar soft-part sarcoma
Inflammatory myofibroblastic tumor
Amyotrophic lateral sclerosis
Young adult-onset Parkinsonism
Extraskeletal Ewing sarcoma
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Precursor T-cell acute lymphoblastic leukemia
Common variable immunodeficiency
Ewing sarcoma
Papillary or follicular thyroid carcinoma
Coffin-Siris syndrome
Peripheral primitive neuroectodermal tumor
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Fibronectin glomerulopathy
Giant cell glioblastoma
Familial isolated dilated cardiomyopathy
Posterior polar cataract
Autosomal dominant nonsyndromic intellectual deficit
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Adult-onset distal myopathy due to VCP mutation
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Atypical juvenile parkinsonism
Clear cell renal carcinoma
MITF-related melanoma and renal cell carcinoma predisposition syndrome
Ocular albinism with congenital sensorineural deafness
Papillary renal cell carcinoma
Tietz syndrome
Waardenburg syndrome type 2
Anaplastic ependymoma
Herpetic encephalitis
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
46,XY partial gonadal dysgenesis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
Hereditary nonpolyposis colon cancer
Hypohidrotic ectodermal dysplasia with immunodeficiency
Familial rhabdoid tumor
Familial multiple meningioma
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Familial ocular anterior segment mesenchymal dysgenesis
Intellectual deficit - sparse hair - brachydactyly
Pseudohypoaldosteronism type 2E
Retinitis pigmentosa
Wolf-Hirschhorn syndrome
Distal 22q11.2 microdeletion syndrome
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxoid / round cell liposarcoma
Cornelia de Lange syndrome
Glucocorticoid resistance
Dent disease type 2
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Oculocerebrorenal syndrome
Aneurysm - osteoarthritis syndrome
Familial thoracic aortic aneurysm and aortic dissection
Familial pancreatic carcinoma
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Huntington disease
Juvenile Huntington disease
Burkitt lymphoma
Microcephaly-capillary malformation syndrome
Estrogen resistance syndrome
Homozygous familial hypercholesterolemia
Osteopetrosis with renal tubular acidosis
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
ADULT syndrome
Acute basophilic leukemia
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Ankyloblepharon - ectodermal defects - cleft lip / palate
Autosomal recessive spastic paraplegia type 20
Bladder exstrophy
EEC syndrome
Incontinentia pigmenti
Intermittent hydrarthrosis
Limb-mammary syndrome
Split hand-split foot malformation
TRAPS syndrome
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
Solitary fibrous tumor
X-linked agammaglobulinemia
22q11.2 deletion syndrome
Acute infantile liver failure-multisystemic involvement syndrome
Acute myeloblastic leukemia without maturation
Acute myeloid leukemia with CEBPA somatic mutations
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive centronuclear myopathy
B-cell chronic lymphocytic leukemia
Brugada syndrome
Cone rod dystrophy
Congenital lactic acidosis, Saguenay-Lac-St. Jean type
Constitutional mismatch repair deficiency syndrome
Cowden syndrome
Craniometaphyseal dysplasia
Desmoid tumor
Desmoplastic small round cell tumor
Extraskeletal myxoid chondrosarcoma
Familial atrial fibrillation
Hepatocellular carcinoma, childhood-onset
Hereditary sensory and autonomic neuropathy type 2
Hypoplastic left heart syndrome
Inherited acute myeloid leukemia
Intellectual deficit, X-linked, Snyder type
Isolated adermatoglyphia
Isolated focal cortical dysplasia type IIb
Leber congenital amaurosis
Meckel syndrome
Melanoma of soft part
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Oculodentodigital dysplasia
Parkinsonian-pyramidal syndrome
Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
Proteus syndrome
Pseudohypoaldosteronism type 2C
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Spinocerebellar ataxia type 19 / 22
Syndactyly type 3
TARP syndrome
Total congenital cataract
Tuberous sclerosis
Weaver 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 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 partial lipodystrophy, Dunnigan type
Familial partial lipodystrophy, Köbberling type
Heart-hand syndrome, Slovenian type
Hutchinson-Gilford progeria syndrome
LMNA-related cardiocutaneous progeria syndrome
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction
Lethal restrictive dermopathy
Mandibuloacral dysplasia with type A lipodystrophy
Progeria-associated arthropathy
Atypical teratoid tumor
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
Neurofibromatosis type 3
Branchio-oculo-facial syndrome
Chronic myeloid leukemia
Hermansky-Pudlak syndrome with neutropenia
Precursor B-cell acute lymphoblastic leukemia
ALDH18A1-related De Barsy syndrome
Action myoclonus - renal failure syndrome
Anauxetic dysplasia
Behçet disease
Cap myopathy
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Digitotalar dysmorphism
Dilated cardiomyopathy with ataxia
Familial isolated congenital asplenia
Fatal infantile cytochrome C oxidase deficiency
Gaucher disease type 1
Leigh syndrome with cardiomyopathy
Leigh syndrome with nephrotic syndrome
Mandibulofacial dysostosis-microcephaly syndrome
Omenn syndrome
Pyruvate dehydrogenase E3 deficiency
Rare isolated myopia
Sheldon-Hall syndrome
T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
Trismus - pseudocamptodactyly
Typical nemaline myopathy
Unverricht-Lundborg disease
- Carcinoma associated with MITF/TFE translocation
- Translocation carcinoma

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

Classification (ICD10):
- Neoplasms -

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

No signs/symptoms info available.