Disease Index

This syndrome is characterised by chronic diarrhoea in infancy or childhood in association with intestinal glucoamylase deficiency

Chronic form of encephalitis

Human disease

human disease

human disease

diverse group of hereditary diseases in which certain cells of the immune system have difficulty forming the reactive oxygen compounds used to kill certain ingested pathogens

Chronic hiccup is a rare movement disorder characterized by involuntary spasmodic contractions of the inspiratory muscles synchronized with larynx closure lasting for more than 48 hours

acquired immune-mediated inflammatory disorder of the peripheral nervous system

medical condition

central nervous system inflammatory disease

lymphoblastic leukemia characterized by over production of B-cells and their accumulation in bone marrow and blood

human disease

myeloid leukemia that is characterized by over production of white blood cells

chronic leukemia characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood

chronic leukemia characterized by neutrophilic leukocytosis with no detectable Philadelphia chromosome or BCR/ABL fusion gene

Chronic pneumonitis of infancy is a rare pediatric form of interstitial lung disease (ILD, see this term)

Chronic form of polyradiculoneuropathy

Chronic primary adrenal insufficiency (CPAI) is a chronic disorder of the adrenal cortex resulting in the inadequate production of glucocorticoid and mineralocorticoid hormones

human disease

osteomyelitis characterized by multiple foci of painful swelling of bones, mainly in the metaphyses of the long bones, in addition to the pelvis, the shoulder girdle and the spine

human disease

medical condition

Chudley-Lowry syndrome is an X-linked mental retardation (XLMR) syndrome belonging to the group of conditions characterised by the association of intellectual deficit with hypotonic facies (Mental retardation-hypotonic facies; see this term)

human disease

genetic disorder caused by a heterozygous mutation along the PHIP gene