Disease Directory

GUCY2D retinopathy is a type of inherited retinal dystrophy that occurs because of a mutation in the GUCY2D gene. This condition affects the retina, w...

GUCY2D-related dominant retinopathy is a type of inherited eye disease that affects the retina, the light-sensitive part of the eye. This condition is...

GUCY2D-related recessive retinopathy is a condition that affects the retina, the light-sensitive tissue at the back of the eye. This condition is caus...

GYG1-related disorder of glycogen metabolism is a rare condition that affects the way the body processes and stores glycogen. This condition is caused...

Gabriele de Vries syndrome, also known as YY1 haploinsufficiency syndrome, GADEVS, Gabriele-De Vries syndrome, or Gabriele-de Vries syndrome, is a rar...

Gaisbock syndrome, also known as Gaisbock's syndrome or stress polycythemia, is a condition where polycythemia develops as a result of stress. This me...

Galloway-Mowat syndrome, also known as Galloway syndrome among other names, is a rare condition that involves problems with both the kidneys and the c...

Galloway-Mowat syndrome 1 is a rare genetic condition that is catalogued in well-known medical resources. Information on the overall description and f...

Galloway-Mowat syndrome 10 (also known as GAMOS10) is a rare genetic condition. Although detailed information about this disorder is limited, it is kn...

Galloway-Mowat syndrome 2, X-linked is a rare genetic condition. It is also known by several names including GAMOS2 and X-linked recessive. Detailed i...

Galloway-Mowat syndrome 3 (also known as GAMOS3) is a rare genetic condition that has been identified by its association with the OSGEP gene. It is ca...

Information about overview is currently limited for this condition.

Galloway-Mowat syndrome 5 (GAMOS5) is a rare condition that has been recognized in scientific databases with the identifier OMIM:617731. While detaile...

Galloway-Mowat syndrome 6, also known as GALLOWAY-MOWAT SYNDROME 6 or GAMOS6, is a rare condition with very limited publicly available information. It...

Galloway-Mowat syndrome 7, also known as GAMOS7, is a rare genetic condition that has been linked to changes in the NUP107 gene. Detailed clinical inf...

Galloway-Mowat syndrome 8 (GAMOS8) is a rare genetic condition that has been linked to changes in the NUP133 gene. This condition is identified in rec...

Galloway-Mowat syndrome 9 (also known as GAMOS9) is a rare genetic condition that has been associated with changes in the GON7 gene. It is recognized...

Gamstorp-Wohlfart syndrome is a rare condition that affects the peripheral nerves. It is a slowly progressive disorder in which the nerve fibers, espe...

Gardner syndrome is a severe form of familial adenomatous polyposis, a condition where many adenomas (small benign tumors) develop in the colon and re...

Garg-Mishra progeroid syndrome is a rare condition that has been noted in medical genetics and is catalogued in OMIM (OMIM:620601). Although detailed...