Experimental Factor Ontology
692 terms(s) returned
Term Type: | Record: 201 to 250 of 692 Records | Page: 5 of 14, First Previous Next Last | Show Records Per Page |
- hereditary antithrombin deficiency
- hereditary arterial and articular multiple calcification syndrome
- hereditary attention deficit-hyperactivity disorder
- hereditary benign intraepithelial dyskeratosis
- hereditary breast carcinoma
- hereditary breast ovarian cancer syndrome
- hereditary cerebellar ataxia
- hereditary chronic pancreatitis
- hereditary clear cell renal cell carcinoma
- hereditary continuous muscle fiber activity
- hereditary coproporphyria
- hereditary cryohydrocytosis with reduced stomatin
- hereditary dementia
- hereditary diffuse gastric adenocarcinoma
- hereditary disorder of connective tissue
- hereditary elliptocytosis
- hereditary endocrine growth disease
- hereditary epidermal appendage anomaly
- hereditary episodic ataxia
- hereditary fallopian tube carcinoma
- hereditary folate malabsorption
- hereditary fructose intolerance
- hereditary gallbladder disorder
- hereditary gastric cancer
- hereditary geniospasm
- hereditary gingival fibromatosis
- hereditary glaucoma
- hereditary hemochromatosis
- hereditary hemolytic uremic syndrome
- hereditary hemophagocytic lymphohistiocytosis
- hereditary hemorrhagic telangiectasia
- hereditary hyperbilirubinemia
- hereditary hypercarotenemia and vitamin A deficiency
- hereditary hyperekplexia
- hereditary hyperferritinemia with congenital cataracts
- hereditary hyperparathyroidism
- hereditary hypoparathyroidism
- hereditary hypophosphatemic rickets
- hereditary hypophosphatemic rickets with hypercalciuria
- hereditary hypotrichosis with recurrent skin vesicles
- hereditary inclusion body myopathy type 4
- hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome
- hereditary inclusion-body myopathy
- hereditary intrinsic factor deficiency
- hereditary kidney oncocytoma
- hereditary leiomyomatosis and renal cell cancer
- hereditary lethal multiple congenital anomalies/dysmorphic syndrome
- hereditary lipodystrophy
- hereditary macular dystrophy
- hereditary methemoglobinemia