Disease Index

Ghosal hematodiaphyseal dysplasia syndrome (GHDD) is a rare disorder characterized by increased bone density (predominantly diaphyseal) and aregenerative corticosteroid-sensitive anemia

human disease

human disease

human disease

glioblastoma multiforme that is characterized by a prevalence of bizarre, multinucleated giant cells

type of mole found in infants at birth

giant cell tumor and bone cancer and bone tissue neoplasm that results in the presence of multinucleated giant cells (osteoclast-like cell)

instance of ossifying fibroma (disease) that is caused by an inherited modification of the individual's genome

human disease which causes the body to grow abnormally large

metabolic disorder in which the liver processes bilirubin slowly

medical condition

human disease

rare condition of gingival overgrowth

human disease

medical condition

Gingival fibromatosis - facial dysmorphism is a very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism

medical condition

Human disease

human disease

medical condition

human disease

Glaucoma-sleep apnea syndrome is characterized by sleep apnoea associated with glaucoma. It has been described in five members of a family (the mother and four of her children).

general term for numerous tumors of the central nervous system

human disease

human disease

type of tumor that starts in the brain or spine

rare primary brain tumor

Human disease