Disease Directory

Information about overview is currently limited for this condition.

EN1-related dorsoventral syndrome is a rare genetic disorder that affects limb development and other body systems. It is characterized by a type of dy...

ENDOVE syndrome, limb-brain type is a rare condition that has been associated with anomalies affecting the limbs and brain. It is also known by the sy...

ENDOVE syndrome, limb-only type (also known as ENDOVESL or Mesomelia of Lower Extremities With Hand and Foot Anomalies) is a rare condition that prima...

EPHB4-related lymphatic-related hydrops fetalis is a rare condition that affects the lymphatic system. This condition is known for its wide range of p...

EYS-related retinopathy is an inherited eye condition that affects the retina, the light-sensitive layer at the back of the eye. It is caused by chang...

EZB diffuse large B-cell lymphoma is a type of diffuse large B-cell lymphoma that is identified by its genetic features. The LymphGen algorithm catego...

EZB-MYC+ diffuse large B-cell lymphoma is a subtype of diffuse large B-cell lymphoma. This condition is characterized by a gene expression profile tha...

EZB-MYC- diffuse large B-cell lymphoma is a type of large B-cell lymphoma identified through gene expression profiling. It is a subtype of EZB diffuse...

Eales disease is an inflammatory condition affecting the veins of the retina. It is characterized by three stages: vasculitis (inflammation of the blo...

East Texas bleeding disorder is a rare condition that has been recognized in several trusted medical resources, including OMIM, Orphanet, and GARD. Al...

Ebola hemorrhagic fever is a serious viral infection caused by the Ebola virus. It is primarily spread by contact with infected animals or people. Thi...

Ebstein anomaly is a rare congenital heart defect. It is characterized by a malformation of the tricuspid valve, where the septal and inferior leaflet...

Edinburgh malformation syndrome is a rare genetic condition that affects multiple parts of the body. People with this condition are born with several...

Ehlers-Danlos syndromes (EDS) are a group of inherited conditions that affect the body’s connective tissue. This connective tissue is important for su...

Information about this condition is currently limited. Ehlers-Danlos syndrome due to tenascin-X deficiency is a rare disorder associated with changes...

Ehlers-Danlos syndrome type 7A (EDS VIIA) is a rare connective tissue disorder that is part of the Ehlers-Danlos syndromes. This condition has been no...

Ehlers-Danlos syndrome, Beasley-Cohen type is a rare condition that is part of the broader group of Ehlers-Danlos syndromes. It is also known by other...

Ehlers-Danlos syndrome, arthrochalasia type is an inherited connective tissue disorder caused by defects in collagen, a protein important for normal t...

Ehlers-Danlos syndrome, arthrochalasia type, 2 (also known as EDS 7B or EDS VIIB) is a rare inherited connective tissue disorder. Although detailed in...