Disease Directory

Colorectal lymphoma is an extranodal lymphoma that arises from the colon or rectum, most often manifesting as a type of B-cell non-Hodgkin lymphoma. T...

Colorectal neuroendocrine tumor G1 is a well differentiated, low grade neoplasm that arises from the colon or rectum. It is characterized by a low mit...

Columnar cell variant thyroid gland papillary carcinoma is a morphologic variant of thyroid cancer marked by pseudostratified malignant follicular cel...

Combined ApoA-I and ApoC-III deficiency is a disorder affecting lipid metabolism that leads to abnormally low levels of high-density lipoprotein, a ke...

Combined PSAP deficiency is an encephalopathy that belongs to the sphingolipidoses group of lysosomal storage diseases. This condition results from ch...

Combined cervical dystonia is a movement disorder affecting the neck muscles, leading to abnormal posturing and involuntary contractions. Although the...

Combined deficiency of factor V and factor VIII is an inherited bleeding disorder characterized by reduced activity and antigen levels of two essentia...

Combined deficiency of factor VII and factor X is a bleeding disorder that affects the blood coagulation system. Due to the rarity of the condition, w...

Combined dystonia, also referred to as dystonia-plus syndrome, is a movement disorder in which involuntary muscle contractions and abnormal posturing...

Combined hamartoma of the retina and retinal pigment epithelium is a rare ocular condition affecting the retina and the underlying pigment epithelium....

Combined hepatocellular carcinoma and cholangiocarcinoma is a rare malignant tumor of the liver that contains features of both hepatocellular carcinom...

Combined hyperactive dysfunction syndrome of the cranial nerves is a neurological condition that appears to affect the function of multiple cranial ne...

Combined immunodeficiency (CID) encompasses a range of inherited disorders that affect both T and B lymphocyte function, leading to increased suscepti...

Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia is a multi-system condition that affects both the immune and h...

Combined immunodeficiency due to CD3gamma deficiency is an extremely rare inherited condition that affects the immune system by impairing the CD3 comp...

Combined immunodeficiency due to CRAC channel dysfunction is a complex disorder that affects the immune system as well as muscle and skin structures....

Combined immunodeficiency due to CTPS1 deficiency is a very rare primary immunodeficiency disorder that affects the immune system by impairing the abi...

Combined immunodeficiency due to DOCK8 deficiency is an inherited immune disorder characterized by defects in both T and B cell function. It is caused...

Combined immunodeficiency due to GINS1 deficiency is a severe immune disorder that also affects growth and development. Affected individuals exhibit m...

Combined immunodeficiency due to LRBA deficiency is an inherited condition that affects the immune system, leading to both recurrent infections and au...