Disease Directory

Eng-Strom syndrome is a rare condition that affects growth and joint movement. It is defined by intrauterine growth retardation, meaning that growth i...

Information about the overview is currently limited for this condition.

Epstein-Barr virus-associated gastric carcinoma (EBVaGC) is a rare form of stomach cancer linked to a latent infection with Epstein-Barr virus (EBV)....

Epstein-Barr virus-associated lymphoproliferative disorder is a group of conditions where certain types of immune cells, such as B cells, T cells, or...

Information about the overview is currently limited for this condition.

Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly is a rare type of blood cancer that mostly affects older people, usually betw...

Epstein-Barr virus-related tumor is a rare type of tumor that is linked to the Epstein-Barr virus (EBV). Although EBV is a common virus, tumors associ...

Erb palsy is a condition that causes a paralysis or significant weakness in the arm. This occurs because of an injury to the upper group of nerves, sp...

Erdheim-Chester disease (ECD) is a rare, multisystemic condition that is classified as a non-Langerhans form of histiocytosis. People with this condit...

Escherichia coli meningitis is a form of gram-negative bacterial meningitis that primarily affects newborns, particularly neonates who are premature o...

Evans syndrome is a rare chronic blood disorder where the body’s immune system mistakenly attacks its own blood cells. People with this condition have...

Ewing sarcoma is a type of cancer that forms a small round cell tumor in bone or soft tissue. It most often affects children and teenagers, particular...

Ewing sarcoma of bone is a small round cell tumor primarily affecting the diaphysis or metaphyseal-diaphyseal regions of long bones. It is characteriz...

Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone is a type of malignant tumor that arises in the bone. These tumors are characterized...

F12-associated cold autoinflammatory syndrome is a rare condition. Information about the disease is currently limited. The condition is listed in reco...

FADD-related immunodeficiency is a rare genetic immune disorder that was initially reported in a single consanguineous Pakistani family. People with t...

FAM20B-congenital disorder of glycosylation is a rare inherited condition that falls under the group of congenital disorders of glycosylation. These d...

Information about the overview is currently limited for this condition.

FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome is a very rare condition. The name suggests that people with this...

FG syndrome 1 is a rare genetic condition that is caused by a mutation in the MED12 gene. It is one member of the FG syndrome spectrum of disorders. M...