Disease Index

human disease

human disease

Odonto-onycho-dermal dysplasia is a form of ectodermal dysplasia characterised by hyperkeratosis and hyperhidrosis of the palms and soles, atrophic malar patches, hypodontia, conical teeth, onychodysplasia, and dry and sparse hair

human disease

medical condition

any of the forms of odontogenic neoplasm

Odontohypophosphatasia (odonto-HPP) is the least severe form of hypophosphatasia (see this term) characterized by premature exfoliation of primary and/or permanent teeth and/or severe dental caries, in the absence of skeletal system abnormalities

Odontoma-dysphagia syndrome is a malformation syndrome, characterized by odontomas (undifferentiated mass of the esophagus) and severe dysphagia

human disease

syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities

X-linked disease resulting from a deficiency in N-terminal acetyltransferase, extreme abrupt behavior, anger issues, characterized by postnatal growth failure with severe delays and dysmorphic features in boys

human disease

neonatoal period electroclinical syndrome that is characterized by tonic spasms and partial seizures

medical condition

Autosomal dominant genetic condition

human disease

human disease

Oligoarticular juvenile arthritis is the most common form of juvenile idiopathic arthritis (JIA), representing nearly 50% of cases

human disease

human disease

medical condition

Oligocone trichromacy is a rare non-progressive form of cone photoreceptor dysfunction characterised by reduced visual acuity, normal retinal appearance, absent or reduced cone responses on electroretinography but normal colour vision

type of glioma that are believed to originate from the oligodendrocytes of the brain or from a glial precursor cell

human disease

reduced number of teeth, whereby more than 6 teeth are missing

renal hypoplasia characterized by bilateral reduced kidney size with a marked decrease in the total number of nephrons

human disease

Oliver syndrome is a very rare syndrome characterized by intellectual deficit, postaxial polydactyly, and epilepsy