Experimental Factor Ontology
94474 terms(s) returned
| Term Type: | Record: 87801 to 87850 of 94474 Records | Page: 1757 of 1890, First Previous Next Last | Show Records Per Page |
- short stature, Brussels type
- short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis
- short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies
- short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1
- short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2
- short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies
- short stature, microcephaly, and endocrine dysfunction
- short stature, oligodontia, dysmorphic facies, and motor delay
- short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay
- short stature-advanced bone age-early-onset osteoarthritis syndrome
- short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
- short stature-brachydactyly-obesity-global developmental delay syndrome
- short stature-craniofacial anomalies-genital hypoplasia syndrome
- short stature-deafness-neutrophil dysfunction-dysmorphism syndrome
- short stature-heart defect-craniofacial anomalies syndrome
- short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
- short stature-optic atrophy-Pelger-Huët anomaly syndrome
- short stature-pituitary and cerebellar defects-small sella turcica syndrome
- short stature-valvular heart disease-characteristic facies syndrome
- short stature-webbed neck-heart disease syndrome
- short stature-wormian bones-dextrocardia syndrome
- short tarsus-absence of lower eyelashes syndrome
- short term hematopoietic stem cell
- short transmembrane mitochondrial protein 1 (human)
- short ulna-dysmorphism-hypotonia-intellectual disability syndrome
- short-chain dehydrogenase/reductase 3
- short-chain dehydrogenase/reductase 3 (human)
- short-chain fatty acyl-CoA dehydrogenase activity
- short-chain specific acyl-CoA dehydrogenase, mitochondrial
- short-chain specific acyl-CoA dehydrogenase, mitochondrial (human)
- short-limb skeletal dysplasia with severe combined immunodeficiency
- short-rib thoracic dysplasia 10 with or without polydactyly
- short-rib thoracic dysplasia 13 with or without polydactyly
- short-rib thoracic dysplasia 14 with polydactyly
- short-rib thoracic dysplasia 16 with or without polydactyly
- short-rib thoracic dysplasia 17 with or without polydactyly
- short-rib thoracic dysplasia 18 with polydactyly
- short-rib thoracic dysplasia 19 with or without polydactyly
- short-rib thoracic dysplasia 20 with polydactyly
- short-rib thoracic dysplasia 21 without polydactyly
- short-rib thoracic dysplasia 22 without polydactyly
- short-rib thoracic dysplasia 6 with or without polydactyly
- short-rib thoracic dysplasia 7/20 with polydactyly, digenic
- short-rib thoracic dysplasia 9 with or without polydactyly
- short-term memory
- short/branched chain specific acyl-CoA dehydrogenase, mitochondrial
- short/branched chain specific acyl-CoA dehydrogenase, mitochondrial (human)
- shorthand
- shortness of breath
- should_conform_to
