Term info
database cross reference
- Orphanet:409941 (MONDO:equivalentTo)
exactMatch
http://purl.obolibrary.org/obo/Orphanet_409941
has exact synonym
not genetically inherited
id
MONDO:0021141
Term relations
Related from:
has characteristic
- acquired color blindness
- acquired hypertrophic pyloric stenosis
- Carney triad
- acquired testicular failure
- acquired Fanconi syndrome
- secondary hemophagocytic lymphohistiocytosis
- acquired aplastic anemia
- acquired thrombocytopenia
- acquired night blindness
- acquired neutropenia
- acquired peripheral neuropathy
- acquired laryngomalacia
- acquired chronic primary adrenal insufficiency
- Meigs syndrome
- acquired hemangioma
- growing teratoma syndrome
- acquired porencephaly
- acquired neuromuscular junction disease
- acquired motor neuron disease
- steroid-responsive encephalopathy associated with autoimmune thyroiditis
- progressive rubella panencephalitis
- acquired hemoglobinopathy
- acquired coagulation factor deficiency
- acquired aneurysmal subarachnoid hemorrhage
- acquired angioedema
- acquired torsion dystonia
- acquired idiopathic torsion dystonia
- acquired primary ovarian failure
- acquired central diabetes insipidus
- acquired pituitary hormone deficiency
- fibrous dysplasia
- acquired prothrombin deficiency
- acquired polycythemia
- acquired ichthyosis
- acquired Creutzfeldt-Jakob disease
- presbycusis
- acquired skeletal muscle disease
- acquired epidermolysis bullosa
- acquired purpura fulminans
- acquired schizencephaly
- non-familial hypertrophic cardiomyopathy
- acquired pseudoxanthoma elasticum
- acquired dermis elastic tissue disorder
- acquired ataxia
- acquired deficiency anemia
- acquired keratosis
- acquired metabolic disease