Experimental Factor Ontology
11113 terms(s) returned
| Term Type: | Record: 1001 to 1050 of 11113 Records | Page: 21 of 223, First Previous Next Last | Show Records Per Page |
- obsolete precancerous lesion of palpebral epidermis
- obsolete prenatal benign hypophosphatasia
- obsolete presynaptic congenital myasthenic syndrome
- obsolete primary bone dysplasia with increased bone density
- obsolete primary bone dysplasia with multiple joint dislocations
- obsolete primary congenital hypothyroidism
- obsolete primary glomerular disease
- obsolete primary hereditary glaucoma
- obsolete primary immunodeficiency due to a defect in adaptive immunity
- obsolete primary immunodeficiency due to a genetic defect in innate immunity
- obsolete primary lipodystrophy
- obsolete primary myoclonus
- obsolete primary parathyroid hyperplasia
- obsolete primary qualitative or quantitative defects of alpha-dystroglycan
- obsolete primary renal tubular acidosis
- obsolete primary short bowel syndrome
- obsolete processed material
- obsolete progressive cerebello-cerebral atrophy
- obsolete proliferative vitreoretinopathy
- obsolete protein glycosylation
- obsolete protein glycosylation in endoplasmic reticulum
- obsolete pulmonary arteriovenous malformation
- obsolete pure or complex X-linked spastic paraplegia
- obsolete pure or complex autosomal dominant spastic paraplegia
- obsolete pure or complex autosomal recessive spastic paraplegia
- obsolete putative T-complex protein 10A homolog (human)
- obsolete putative uncharacterized protein TXNRD3NB (human)
- obsolete qualitative or quantitative defects of calpain
- obsolete qualitative or quantitative defects of emerin
- obsolete qualitative or quantitative defects of fukutin
- obsolete qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
- obsolete qualitative or quantitative defects of integrin alpha-7
- obsolete qualitative or quantitative defects of merosin
- obsolete qualitative or quantitative defects of myotilin
- obsolete qualitative or quantitative defects of myotubularin
- obsolete qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase
- obsolete qualitative or quantitative defects of protein glycosyltransferase-like
- obsolete qualitative or quantitative defects of troponin
- obsolete radiation or chemically induced disorder
- obsolete rare constitutional hemolytic anemia due to an enzyme disorder
- obsolete rare developmental defect with connective tissue involvement
- obsolete rare disease with dentinogenesis imperfecta
- obsolete rare disease with glaucoma as a major feature
- obsolete rare disorder with congenital hypogonadotropic hypogonadism
- obsolete rare disorder with dystonia and other neurologic or systemic manifestation
- obsolete rare eye disease due to a differentiation anomaly
- obsolete rare eyelid malformation
- obsolete rare familial disorder with hypertrophic cardiomyopathy
- obsolete rare female infertility due to adrenal disorder of genetic origin
- obsolete rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
