Experimental Factor Ontology
926 terms(s) returned
Term Type: | Record: 701 to 750 of 926 Records | Page: 15 of 19, First Previous Next Last | Show Records Per Page |
- mucopolysaccharidosis type 3
- mucopolysaccharidosis type 3A
- mucopolysaccharidosis type 3B
- mucopolysaccharidosis type 3C
- mucopolysaccharidosis type 3D
- mucopolysaccharidosis type 4
- mucopolysaccharidosis type 4A
- mucopolysaccharidosis type 4B
- mucopolysaccharidosis type 6
- mucopolysaccharidosis type 6, rapidly progressing
- mucopolysaccharidosis type 6, slowly progressing
- mucopolysaccharidosis type 7
- mucopolysaccharidosis type 9
- mucopolysaccharidosis-plus syndrome
- mucosal melanoma
- mucosulfatidosis
- mulibrey nanism
- mullerian aplasia
- mullerian aplasia and hyperandrogenism
- mullerian derivatives-lymphangiectasia-polydactyly syndrome
- mullerian duct anomalies-limb anomalies syndrome
- multi-infarct dementia
- multicentric carpo-tarsal osteolysis with or without nephropathy
- multicentric osteolysis-nodulosis-arthropathy spectrum
- multicystic dysplastic kidney
- multifocal dystonia
- multifocal pattern dystrophy simulating fundus flavimaculatus
- multiminicore myopathy
- multinodular goiter
- multinodular goiter-cystic kidney-polydactyly syndrome
- multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome
- 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 carboxylase deficiency
- 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