Experimental Factor Ontology
11043 terms(s) returned
| Term Type: | Record: 1001 to 1050 of 11043 Records | Page: 21 of 221, First Previous Next Last | Show Records Per Page |
- 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
- obsolete rare genetic bone development disorder
- obsolete rare genetic disease with myoclonus as a major feature
- obsolete rare genetic disorder with obstructive azoospermia
- obsolete rare genetic hypothalamic or pituitary disease
- obsolete rare genetic parathyroid disease and phosphocalcic metabolism disorder
- obsolete rare genetic refraction anomaly
- obsolete rare hemorrhagic disorder due to a constitutional coagulation factors defect
- obsolete rare hereditary disease with avascular necrosis
- obsolete rare hereditary disease with peripheral neuropathy
- obsolete rare hereditary metabolic disease with peripheral neuropathy
- obsolete rare hereditary neurologic disease with peripheral neuropathy
- obsolete rare hereditary systemic disease with peripheral neuropathy
- obsolete rare hereditary thrombophilia
- obsolete rare hyperopia and astigmatism
- obsolete rare insulin-resistance syndrome
- obsolete rare male infertility due to adrenal disorder of genetic origin
- obsolete rare male infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin
- obsolete rare male infertility due to testicular endocrine disorder
- obsolete rare odontal or periodontal disorder
- obsolete rare otorhinolaryngological malformation
- obsolete rare parkinsonian syndrome due to genetic neurodegenerative disease
- obsolete rare paroxysmal movement disorder
- obsolete rare strabismus and restriction syndrome
- obsolete rare syndrome with cardiac malformations
- obsolete recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome
- obsolete regenerating islet-derived protein 3-gamma
- obsolete reproduction
