Disease Index

Cernunnos-XLF deficiency is a rare form of combined immunodeficiency characterized by microcephaly, growth retardation, and T and B cell lymphopenia

cervix carcinoma that derives from epithelial cells of glandular origin

cervical carcinosarcoma that is located in the cervix

human disease

human disease

Human disease

human disease

human disease

cervix carcinoma that has material basis in squamous cells of the cervix

human disease

human disease

human disease

cancer arising from the cervix

human disease

human disease

Human disease

diseases caused by disturbed function of ion channel subunits or the proteins that regulate them

human disease

viral infectious disease that is a hemorrhagic fever, has material basis in Chapare virus. The infection has symptom headache, has symptom joint pain, has symptom muscle pain, has symptom vomiting, has symptom shock, and has symptom bleeding

patent ductus arteriosus with facial dysmorphism and abnormal fifth digits

Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the DYNC1H1 gene on chromosome 14q32

Charcot-Marie-Tooth disease type 2 that has material basis in heterozygous mutation in the TRPV4 gene on chromosome 12q24

Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the gene encoding heat-shock 27-kD protein-1 (HSPB1)

human disease

Charcot-Marie-Tooth disease type 2 that has material basis in variation in the region 8q13-q23

Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the GDAP1 gene on chromosome 8q

Charcot-Marie-Tooth disease type 2 that has material basis in mutation in the HSPB8 gene