Term with siblings
dopamine beta-hydroxylase deficiency

amino acid metabolic disorder +
aromatic L-amino acid decarboxylase deficiency
arthrogryposis multiplex congenita +
autoimmune disease of the nervous system +
Behr syndrome
bilirubin metabolic disorder +
carbohydrate metabolic disorder +
central nervous system disease +
cerebral amyloid angiopathy +
congenital nervous system abnormality +
D-glyceric aciduria
diplegia of upper limb
familial hypocalciuric hypercalcemia +
familial visceral amyloidosis
Gerstmann syndrome
glycerol kinase deficiency
Gordon Holmes syndrome
Greenberg dysplasia
herpes zoster
HRPT-related hyperuricemia
hyperekplexia +
hyperphosphatemic familial tumoral calcinosis
hypoinsulinemic hypoglycemia with hemihypertrophy
immunoglobulin light chain amyloidosis
isolated elevated serum creatine phosphokinase levels
isolated sulfite oxidase deficiency
lipid metabolism disorder +
locked-in syndrome
lysosomal storage disease +
metal metabolism disorder +
mitochondrial metabolism disease +
multiple acyl-CoA dehydrogenase deficiency
nervous system benign neoplasm +
nervous system cancer +
neuroleptic malignant syndrome
peripheral nervous system disease +
peroxisomal disease +
phosphoribosylpyrophosphate synthetase superactivity
plasma protein metabolism disease +
porphyria +
primary cutaneous amyloidosis +
purine-pyrimidine metabolic disorder +
pyrimidine metabolic disorder +
sensory system disease +
spinocerebellar ataxia type 1 with axonal neuropathy
thiopurine S-methyltransferase deficiency
toxic encephalopathy
transthyretin amyloidosis
variant ABeta2M amyloidosis
vitamin metabolic disorder +
warfarin resistance
warfarin sensitivity
X-linked warfarin sensitivity
Child term(s)

is-a denotes an 'is-a' relationship