Disease Directory

Ehlers-Danlos syndrome, autosomal dominant, type unspecified is a rare condition that is not fully detailed in the current literature. It is also know...

Ehlers-Danlos syndrome, cardiac valvular type is a genetic condition that affects the connective tissues in the body. This form of the syndrome is mar...

Ehlers-Danlos syndrome, classic type is a connective tissue condition characterized by highly elastic and fragile skin accompanied by widened, atrophi...

Ehlers-Danlos syndrome, classic type, 1 is a condition caused by a mutation in the COL5A1 gene. This mutation affects the body’s ability to produce no...

Ehlers-Danlos syndrome, classic type, 2 is a form of Ehlers-Danlos syndrome caused by a mutation in the COL5A2 gene. People with this condition have a...

Ehlers-Danlos syndrome, classic-like, 2 is a rare genetic disorder that affects the body’s connective tissue. Although a detailed definition is not av...

Ehlers-Danlos syndrome, classic-like, 3 is a rare condition that affects connective tissues in the body. Although detailed information about the condi...

Ehlers-Danlos syndrome, dermatosparaxis type is a form of Ehlers-Danlos syndrome that affects the skin. This condition is marked by extreme skin fragi...

Ehlers-Danlos syndromes (EDS) are a group of inherited disorders that affect the connective tissues. People with this type, known as fibronectinemic t...

Ehlers-Danlos syndrome, hypermobility type is a connective tissue condition characterized primarily by joint hyperlaxity, mild skin hyperextensibility...

Ehlers-Danlos syndrome, kyphoscoliotic type 1 is a rare form of Ehlers-Danlos syndrome. It is known for causing severe muscle weakness (hypotonia) and...

Ehlers-Danlos syndrome, kyphoscoliotic type, 2 is a rare connective tissue disorder that affects the muscles and joints. People with this condition ar...

Ehlers-Danlos syndrome, musculocontractural type is a congenital form of Ehlers-Danlos syndrome. It is defined by distinct craniofacial features as we...

Ehlers-Danlos syndrome, musculocontractural type 1 (EDSMC1) is a rare genetic condition that affects connective tissue. It is known by several names,...

Ehlers-Danlos syndrome, musculocontractural type 2 is a multisystem connective tissue disorder caused by mutations in the DSE gene. The condition is c...

Ehlers-Danlos syndrome, periodontal type 1 is a rare condition that has been described in the medical literature. It is also known by several other na...

Ehlers-Danlos syndrome, periodontal type 2 is a rare form of Ehlers-Danlos syndrome that may affect the tissues in the periodontium, which support the...

Ehlers-Danlos syndromes (EDS) are a group of inherited conditions that affect the body's connective tissues. These tissues support the skin, bones, bl...

Ehlers-Danlos syndrome, spondylocheirodysplastic type is a rare form of Ehlers-Danlos syndrome that affects connective tissue. It is marked by skeleta...

Ehlers-Danlos syndrome, spondylodysplastic type is a form of Ehlers-Danlos syndrome. It is characterized by features that include signs of premature a...