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Hereditary pheochromocytoma-paraganglioma
6 OMIM references -
7 associated genes
58 connected diseases
No signs/symptoms info
Disease Type of connection
Carney-Stratakis syndrome
Cowden syndrome
Gastrointestinal stromal tumor
Isolated succinate-CoQ reductase deficiency
Carcinoid tumor and carcinoid syndrome
Familial isolated dilated cardiomyopathy
Leigh syndrome with leukodystrophy
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Feingold syndrome type 1
Neuroblastoma
Constitutional mismatch repair deficiency syndrome
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Aneurysm - osteoarthritis syndrome
Familial pancreatic carcinoma
Familial thoracic aortic aneurysm and aortic dissection
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Myhre syndrome
Helicoid peripapillary chorioretinal degeneration
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Autosomal dominant secondary polycythemia
Multiple paragangliomas associated with polycythemia
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Syndromic X-linked intellectual deficit due to JARID1C mutation
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
FTH1-related iron overload
Inherited acute myeloid leukemia
Dedifferentiated liposarcoma
Familial dysautonomia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Well-differentiated liposarcoma
Williams syndrome
X-linked dystonia-parkinsonism
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures
Autosomal dominant nonsyndromic intellectual deficit
Amyotrophic lateral sclerosis
Autosomal agammaglobulinemia
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Lissencephaly due to TUBA1A mutation
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Precursor B-cell acute lymphoblastic leukemia
Acromegaly
Charcot-Marie-Tooth disease type 4G
Familial isolated pituitary adenoma
Hypomyelination with atrophy of basal ganglia and cerebellum
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Non-spherocytic hemolytic anemia due to hexokinase deficiency
Primary dystonia, DYT4 type
Spinocerebellar ataxia type 26
Succinyl-CoA:3-ketoacid CoA transferase deficiency
Synonym(s):
- Familial pheochromocytoma-paraganglioma
- SDHx-related paraganglioma-pheochromocytoma
Classification (Orphanet):
- Rare circulatory system disease
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal dominant
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.