Additional Disease Briefs

chronic pneumonitis of infancy

Also known as: CPI

chronic primary adrenal insufficiency

Also known as: Addison disease, Addison disease, chronic adrenal insufficiency, Addison's disease, CPAI, adrenal aplasia, adrenal gland hypofunction, adrenal hypoplasia, autoimmune Addison disease, autoimmune adrenalitis, autoimmune primary adrenal insufficiency, chronic adrenocorticoid insufficiency, classic Addison's disease, hypoadrenocorticism familial, hypoadrenocorticism, familial, primary Addison's disease, primary adrenal insufficiency, chronic, primary adrenocortical insufficiency, primary hypoadrenalism

chronic rapidly progressive glomerulonephritis

Also known as: chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis, rapidly progressive glomerulonephritis, chronicchronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis, rapidly progressive glomerulonephritis, chronic

chronic recurrent multifocal osteomyelitis

Also known as: CMO, CNO/CRMO, CRMO, NBO, chronic multifocal osteomyelitis, chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis, chronic recurrent multifocal osteomyelitis, chronic recurrent multifocal osteomyelitis (disease), multifocal osteomyelitis, chronic, non-bacterial osteomyelitis, osteomyelitis, chronic multifocal

chronic relapsing inflammatory optic neuropathy

Also known as: CRION, chronic recurrent isolated optic neuritis

chronic respiratory distress with surfactant metabolism deficiency

chronic thromboembolic pulmonary hypertension

Also known as: CTEPH, Cteph, Dvt-negative, susceptibility to, pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to

Chudley-McCullough syndrome

Also known as: CMCS, Chudley-McCullough syndrome, deafness, autosomal recessive 82, deafness, autosomal recessive 82, formerly, deafness, bilateral sensorineural, and hydrocephalus due to foramen of Monro obstruction, deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts

Chuvash polycythemia

Also known as: Chuvash erythrocytosis, Chuvash erythromatosis, Chuvash polycythemia, Chuvash type polycythemia, ECYT2, VHL familial polycythemia, Von Hippel-Lindau-dependent polycythemia, autosomal recessive benign erythrocytosis, erythrocytosis, autosomal recessive benign, erythrocytosis, familial, 2, erythrocytosis, familial, type 2, familial erythrocytosis 2, familial polycythemia caused by mutation in VHL, polycythemia, Chuvash type, polycythemia, VHL-dependent

chylomicron retention disease

Also known as: Anderson disease, CMRD, CRD, chylomicron retention disease, hypobetalipoproteinemia with accumulation of apolipoprotein B-like Protein in intestinal cells, hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells, lipid Transport defect of intestine