Mondo Disease Ontology
5944 terms(s) returned
| Term Type: | Record: 2401 to 2450 of 5944 Records | Page: 49 of 119, First Previous Next Last | Show Records Per Page |
- obsolete hemorrhagic disorder due to a qualitative platelet defect
- obsolete hemorrhagic disorder due to an acquired coagulation factor defect
- obsolete hemorrhagic disorder due to an acquired platelet anomaly
- obsolete hemorrhagic syndrome, bovine
- obsolete hepatic veno-occlusive disease
- obsolete hepatitis b vaccine, response to
- obsolete hepatitis delta
- obsolete hepatoblastoma
- obsolete hepatoblastoma
- obsolete hepatocellular adenoma
- obsolete hepatoerythropoietic porphyria
- obsolete hepatoid adenocarcinoma
- obsolete hereditary 46,XX disorder of sex development
- obsolete hereditary 46,XY disorder of sex development
- obsolete hereditary ATTR amyloidosis
- obsolete hereditary acrokeratotic poikiloderma of Kindler-Weary
- obsolete hereditary alopecia
- obsolete hereditary angioedema
- obsolete hereditary angioedema with normal C1Inh
- obsolete hereditary ataxia
- obsolete hereditary biliary tract disease
- obsolete hereditary breast and ovarian cancer syndrome
- obsolete hereditary capillary infantile hemangioma
- obsolete hereditary cardiac anomaly
- obsolete hereditary dentin defect
- obsolete hereditary diffuse leukoencephalopathy with axonal spheroids and pigmented glia
- obsolete hereditary epidermolysis bullosa associated with ocular features
- obsolete hereditary eye tumor
- obsolete hereditary fructose intolerance syndrome
- obsolete hereditary gastro-esophageal disease
- obsolete hereditary head and neck malformation
- obsolete hereditary inflammatory or rheumatoid-like osteoarthropathy
- obsolete hereditary intestinal polyposis
- obsolete hereditary isolated aplastic anemia
- obsolete hereditary late onset Parkinson disease
- obsolete hereditary mixed dermis disorder
- obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum
- obsolete hereditary myoglobinuria
- obsolete hereditary night blindness
- obsolete hereditary non-syndromic obesity
- obsolete hereditary otorhinolaryngological malformation
- obsolete hereditary parenchymatous liver disease
- obsolete hereditary pediatric Behçet-like disease
- obsolete hereditary persistence of alpha-fetoprotein
- obsolete hereditary posterior fossa malformation
- obsolete hereditary predisposition to infections
- obsolete hereditary retinal dystrophy
- obsolete hereditary sensory and autonomic neuropathy type 1B
- obsolete hereditary sensory neuropathy
- obsolete hereditary spastic paraplegia
