Experimental Factor Ontology
2722 terms(s) returned
| Term Type: | Record: 1201 to 1250 of 2722 Records | Page: 25 of 55, First Previous Next Last | Show Records Per Page |
- ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
- ectodermal dysplasia 17 with or without limb malformations
- ectodermal dysplasia 7, hair/nail type
- ectodermal dysplasia WNT10A related
- ectodermal dysplasia and immune deficiency
- ectodermal dysplasia and immunodeficiency 1
- ectodermal dysplasia and immunodeficiency 2
- ectodermal dysplasia syndrome
- ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies
- ectodermal dysplasia with natal teeth, Turnpenny type
- ectodermal dysplasia, trichoodontoonychial type
- ectodermal dysplasia-blindness syndrome
- ectodermal dysplasia-cutaneous syndactyly syndrome
- ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
- ectodermal dysplasia-sensorineural deafness syndrome
- ectodermal dysplasia-syndactyly syndrome
- ectodermal placode development
- ectodysplasin-A
- ectodysplasin-A (human)
- ectodysplasin-A proteolytic cleavage product
- ectodysplasin-a, secreted form measurement
- ectoine
- ectoine measurement
- ectomesenchymoma
- ectonucleoside triphosphate diphosphohydrolase 1
- ectonucleoside triphosphate diphosphohydrolase 1 (human)
- ectonucleoside triphosphate diphosphohydrolase 1 measurement
- ectonucleoside triphosphate diphosphohydrolase 2
- ectonucleoside triphosphate diphosphohydrolase 2 (human)
- ectonucleoside triphosphate diphosphohydrolase 3
- ectonucleoside triphosphate diphosphohydrolase 3 (human)
- ectonucleoside triphosphate diphosphohydrolase 3 measurement
- ectonucleoside triphosphate diphosphohydrolase 5 measurement
- ectonucleoside triphosphate diphosphohydrolase 6
- ectonucleoside triphosphate diphosphohydrolase 6 (human)
- ectonucleoside triphosphate diphosphohydrolase 6 measurement
- ectonucleotide pyrophosphatase/phosphodiesterase family member 3
- ectonucleotide pyrophosphatase/phosphodiesterase family member 3 (human)
- ectonucleotide pyrophosphatase/phosphodiesterase family member 3 amount in blood
- ectonucleotide pyrophosphatase/phosphodiesterase family member 5
- ectonucleotide pyrophosphatase/phosphodiesterase family member 5 (human)
- ectonucleotide pyrophosphatase/phosphodiesterase family member 5 measurement
- ectonucleotide pyrophosphatase/phosphodiesterase family member 7
- ectonucleotide pyrophosphatase/phosphodiesterase family member 7 (human)
- ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement
- ectonucleotide pyrophosphatase/phosphodiesterase family member 7, signal peptide removed form
- ectonucleotide pyrophosphatase/phosphodiesterase family member 7, signal peptide removed form (human)
- ectopia lentis 1, isolated, autosomal dominant
- ectopia lentis-chorioretinal dystrophy-myopia syndrome
- ectopic hormone secretion syndrome associated with neoplasia
