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Melanoma and neural system tumor syndrome
1 OMIM reference -
1 associated gene
75 connected diseases
No signs/symptoms info
Disease Type of connection
Familial pancreatic carcinoma
Familial melanoma
Precursor B-cell acute lymphoblastic leukemia
Precursor T-cell acute lymphoblastic leukemia
Melanoma-pancreatic cancer syndrome
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
B-cell chronic lymphocytic leukemia
Baraitser-Winter syndrome
Ear-patella-short stature syndrome
Blackfan-Diamond anemia
Autosomal recessive primary microcephaly
Mantle cell lymphoma
Multiple myeloma
Adrenocortical carcinoma
Chuvash erythrocytosis
Essential thrombocythemia
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Von Hippel-Lindau disease
Intellectual deficit, X-linked, Turner type
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Burkitt lymphoma
Autosomal dominant distal renal tubular acidosis
Distal renal tubular acidosis with anemia
Hereditary spherocytosis
Intellectual deficit, X-linked, Nascimento type
Southeast Asian ovalocytosis
Coffin-Siris syndrome
Familial rhabdoid tumor
Werner syndrome
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
Bladder exstrophy
Developmental malformations - deafness - dystonia
EEC syndrome
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Lennox-Gastaut syndrome
Limb-mammary syndrome
Lissencephaly due to TUBA1A mutation
MACS syndrome
Methylcobalamin deficiency type cblG
Spinocerebellar ataxia type 26
Split hand-split foot malformation
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Early-onset progressive neurodegeneration - blindness - ataxia - spasticity
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Feingold syndrome type 1
Fibronectin glomerulopathy
Infantile Refsum disease
Intermediate nemaline myopathy
Neonatal adrenoleukodystrophy
Seckel syndrome
Severe congenital nemaline myopathy
Squamous cell carcinoma of head and neck
Triose phosphate-isomerase deficiency
Typical nemaline myopathy
Young adult-onset Parkinsonism
Zellweger syndrome
Multiple endocrine neoplasia type 1
- Melanoma-astrocytoma syndrome

Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
(no data available)

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

Gene symbol UniProt reference OMIM reference
CDKN2A P42771600160
No signs/symptoms info available.