Disease Directory

Acrofrontofacionasal dysostosis 1 is a very rare condition with limited available information. The condition is listed in medical databases like OMIM...

Acrofrontofacionasal dysostosis 2 is a very rare syndrome that affects the structure of the face, nose, and skull. The condition is characterized by a...

Acrogeria is a congenital skin condition characterized by premature aging, particularly seen as unusually fragile and thin skin on the hands and feet....

Acrokeratosis verruciformis is a rare genetic skin condition characterized by a problem with how the skin forms and renews its outer layer. People wit...

Acromegaloid facial appearance syndrome is a rare condition that affects many parts of the body. People with this condition often have a coarse, acrom...

Acromegaly is an acquired disorder caused by excessive production of growth hormone, usually because of a benign pituitary tumor. It leads to progress...

Acromelanosis is a condition that causes dark patches of skin pigmentation. It is a congenital condition, which means it is present from birth or appe...

Information about acromelic dysplasia is currently limited for this condition.

Acromelic frontonasal dysostosis is a rare form of frontonasal dysplasia. This condition is marked by a combination of distinct craniofacial, brain, a...

Acromesomelic dysplasia is a very rare, inherited condition that affects the bones and leads to a form of short-limb dwarfism. This condition is chara...

Acromesomelic dysplasia 1, Maroteaux type is a rare genetic condition that affects the growth of bones. It is characterized by severe dwarfism with an...

Acromesomelic dysplasia 2A is a rare genetic condition that affects bone development. This condition mainly causes severe dwarfism at birth with abnor...

Acromesomelic dysplasia 2B, also known as Du Pan syndrome, fibular hypoplasia and complex brachydactyly, or fibular aplasia-complex brachydactyly synd...

Acromesomelic dysplasia, Hunter-Thompson type is a rare genetic condition that leads to severe dwarfism, with adult height around 120 cm. People with...

Acromesomelic dysplasia 3 is a rare condition that affects skeletal development. It is also known by several other names, including AMDD and Demirhan...

Acromesomelic dysplasia 4 (AMD4) is a rare skeletal condition that primarily affects the growth of the long bones in the limbs. Although detailed desc...

acromesomelic dysplasia, Campailla Martinelli type is a rare disease. Detailed information about this condition is currently limited in medical litera...

Acroosteolysis is a rare condition characterized by the degeneration of the distal phalanges, which are the bones at the tips of the fingers. This pro...

Acroosteolysis dominant type is a rare genetic condition that affects the bones. This condition is known for the loss of bone tissue in the fingertips...

Acroosteolysis-keloid-like lesions-premature aging syndrome is a rare condition that has been reported under several names, including premature ageing...