Experimental Factor Ontology
4222 terms(s) returned
| Term Type: | Record: 3701 to 3750 of 4222 Records | Page: 75 of 85, First Previous Next Last | Show Records Per Page |
- multifocal pattern dystrophy simulating fundus flavimaculatus
- multifunctional methyltransferase subunit TRM112-like protein
- multifunctional methyltransferase subunit TRM112-like protein (human)
- multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3
- multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 (human)
- multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3, signal peptide removed form (human)
- multifunctional protein ADE2 measurement
- multimerin-2
- multimerin-2 (human)
- multimerin-2 measurement
- multimerin-2, signal peptide removed form (human)
- multiminicore myopathy
- multinodular goiter
- multinodular goiter-cystic kidney-polydactyly syndrome
- multinuclear odontoclast
- multinuclear osteoclast
- multinucleated giant cell
- multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
- multiple PDZ domain protein
- multiple PDZ domain protein (human)
- multiple PDZ domain protein measurement
- multiple acyl-CoA dehydrogenase deficiency
- multiple acyl-CoA dehydrogenase deficiency, mild type
- multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
- multiple benign circumferential skin creases on limbs
- multiple benign circumferential skin creases on limbs 1
- multiple births measurement
- multiple bone fractures
- multiple carboxylase deficiency
- multiple chemical sensitivity
- multiple coagulation factor deficiency protein 2
- multiple coagulation factor deficiency protein 2 (human)
- multiple coagulation factor deficiency protein 2 measurement
- multiple coagulation factor deficiency protein 2, signal peptide removed form (human)
- multiple congenital anomalies due to 14q32.2 imprinting defect
- multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
- multiple congenital anomalies-hypotonia-seizures syndrome
- multiple congenital anomalies-hypotonia-seizures syndrome 1
- multiple congenital anomalies-hypotonia-seizures syndrome 2
- multiple congenital anomalies-hypotonia-seizures syndrome 3
- multiple congenital anomalies-neurodevelopmental syndrome, X-linked
- multiple congenital anomalies/dysmorphic syndrome
- multiple congenital anomalies/dysmorphic syndrome without intellectual disability
- multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
- multiple cutaneous and mucosal venous malformations
- multiple endocrine neoplasia
- multiple endocrine neoplasia type 1
- multiple endocrine neoplasia type 2
- multiple endocrine neoplasia type 2A
