Experimental Factor Ontology
93744 terms(s) returned
| Term Type: | Record: 87001 to 87050 of 93744 Records | Page: 1741 of 1875, First Previous Next Last | Show Records Per Page |
- serum paraoxonase/arylesterase 1 (human)
- serum paraoxonase/arylesterase 1 level
- serum paraoxonase/arylesterase 1, initiator methionine removed form
- serum paraoxonase/arylesterase 1, initiator methionine removed form (human)
- serum paraoxonase/arylesterase 2
- serum paraoxonase/arylesterase 2 (human)
- serum paraoxonase/lactonase 3
- serum paraoxonase/lactonase 3 (human)
- serum protein amount
- serum response factor-binding protein 1
- serum response factor-binding protein 1 (human)
- serum selenium amount
- serum urea amount
- serum zinc amount
- sesquipedalian-2
- sesquipedalian-2 (human)
- sessile serrated polyp
- sessile serrated polyposis cancer syndrome
- set1/Ash2 histone methyltransferase complex subunit ASH2 measurement
- setariasis
- severe Canavan disease
- severe X-linked intellectual disability, Gustavson type
- severe X-linked mitochondrial encephalomyopathy
- severe achondroplasia-developmental delay-acanthosis nigricans syndrome
- severe acute respiratory syndrome
- severe aplastic anemia
- severe combined immunodeficiency
- severe combined immunodeficiency due to CARD11 deficiency
- severe combined immunodeficiency due to CARMIL2 deficiency
- severe combined immunodeficiency due to CD70 deficiency
- severe combined immunodeficiency due to CORO1A deficiency
- severe combined immunodeficiency due to DCLRE1C deficiency
- severe combined immunodeficiency due to DNA-PKcs deficiency
- severe combined immunodeficiency due to IKK2 deficiency
- severe combined immunodeficiency due to LAT deficiency
- severe combined immunodeficiency due to LCK deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- severe congenital hypochromic anemia with ringed sideroblasts
- severe congenital nemaline myopathy
- severe congenital neutropenia
- severe cutaneous adverse reaction
- severe dermatitis-multiple allergies-metabolic wasting syndrome
- severe early-childhood-onset retinal dystrophy
- severe early-onset axonal neuropathy due to MFN2 deficiency
- severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
- severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
- severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome
- severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
- severe hemophilia A
