DisGeNET - a database of gene-disease associations

Source: BEFREE

Diseases associated to Variant: rs201920319 ×

Results per page

Gene

Disease

Variant

Source

Semantic type

Disease Class

Type

HPO Term

DO Class

CUI	Disease	Type	Disease Class	Semantic type	DO Class	HPO Term	Num. genes	Num. SNPs
C0740279	Cerebellar atrophy	disease		Disease or Syndrome		Abnormality of the nervous system	104	21
C0234132	Pyramidal sign	phenotype	Pathological Conditions, Signs and Symptoms; Nervous System Diseases	Sign or Symptom		Abnormality of the nervous system	32	5
C0742038	Cerebellar signs	phenotype		Sign or Symptom		Abnormality of the nervous system	24	5
C0852975	Congenital cerebellar ataxia	disease		Disease or Syndrome			8	2