Human Disease Ontology
844 terms(s) returned
| Term Type: | Record: 301 to 350 of 844 Records | Page: 7 of 17, First Previous Next Last | Show Records Per Page |
- hepatocellular clear cell carcinoma
- hepatocyte
- hepatoerythropoietic porphyria
- hepatoid adenocarcinoma
- hepatoid pattern ovarian yolk sac tumor
- hepatoid pattern testicular yolk sac tumor
- hepatomegaly
- hepatopancreatic ampulla
- hepatopulmonary syndrome
- hepatorenal syndrome
- hepatosplenic T-cell lymphoma
- hepatosplenomegaly
- herb food product
- hereditary Wilms' tumor
- hereditary alpha tryptasemia syndrome
- hereditary angioedema
- hereditary angioedema type I
- hereditary angioedema type III
- hereditary arterial and articular multiple calcification syndrome
- hereditary ataxia
- hereditary breast ovarian cancer syndrome
- hereditary choroidal atrophy
- hereditary combined deficiency of vitamin K-dependent clotting factors
- hereditary conventional renal cell carcinoma
- hereditary coproporphyria
- hereditary desmoid disease
- hereditary diffuse gastric cancer
- hereditary elliptocytosis
- hereditary folate malabsorption
- hereditary fructose intolerance syndrome
- hereditary hemorrhagic telangiectasia
- hereditary hypophosphatemic rickets with hypercalciuria
- hereditary lymphedema
- hereditary lymphedema I
- hereditary lymphedema IA
- hereditary lymphedema IB
- hereditary lymphedema IC
- hereditary lymphedema ID
- hereditary lymphedema II
- hereditary mixed polyposis syndrome
- hereditary mixed polyposis syndrome 1
- hereditary mixed polyposis syndrome 2
- hereditary multiple exostoses
- hereditary neuropathy with liability to pressure palsies
- hereditary neutrophilia
- hereditary night blindness
- hereditary nonpolyposis colorectal cancer type 2
- hereditary nonpolyposis colorectal cancer type 4
- hereditary nonpolyposis colorectal cancer type 5
- hereditary nonpolyposis colorectal cancer type 6
