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Multiple endocrine neoplasia type 4
1 OMIM reference -
1 associated gene
39 connected diseases
No signs/symptoms info
Disease Type of connection
Multiple endocrine neoplasia type 1
Lymphangioleiomyomatosis
Tuberous sclerosis
Dedifferentiated liposarcoma
Familial melanoma
Well-differentiated liposarcoma
B-cell chronic lymphocytic leukemia
Mantle cell lymphoma
Multiple myeloma
Cowden syndrome
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Proteus syndrome
Young adult-onset Parkinsonism
Autosomal recessive primary microcephaly
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Isolated focal cortical dysplasia type IIb
Angelman syndrome
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Chronic myeloid leukemia
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Lennox-Gastaut syndrome
Autoimmune lymphoproliferative syndrome with recurrent infections
X-linked distal arthrogryposis multiplex congenita
Synonym(s):
- MEN4
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CDKN1B P46527600778
No signs/symptoms info available.