Experimental Factor Ontology
94474 terms(s) returned
| Term Type: | Record: 3901 to 3950 of 94474 Records | Page: 79 of 1890, First Previous Next Last | Show Records Per Page |
- Autosomal recessive spastic paraplegia type 14
- Autosomal recessive spastic paraplegia type 15
- Autosomal recessive spastic paraplegia type 18
- Autosomal recessive spastic paraplegia type 23
- Autosomal recessive spastic paraplegia type 24
- Autosomal recessive spastic paraplegia type 25
- Autosomal recessive spastic paraplegia type 26
- Autosomal recessive spastic paraplegia type 27
- Autosomal recessive spastic paraplegia type 28
- Autosomal recessive spastic paraplegia type 30
- Autosomal recessive spastic paraplegia type 32
- Autosomal recessive spastic paraplegia type 35
- Autosomal recessive spastic paraplegia type 39
- Autosomal recessive spastic paraplegia type 43
- Autosomal recessive spastic paraplegia type 44
- Autosomal recessive spastic paraplegia type 45
- Autosomal recessive spastic paraplegia type 46
- Autosomal recessive spastic paraplegia type 48
- Autosomal recessive spastic paraplegia type 49
- Autosomal recessive spastic paraplegia type 53
- Autosomal recessive spastic paraplegia type 54
- Autosomal recessive spastic paraplegia type 55
- Autosomal recessive spastic paraplegia type 56
- Autosomal recessive spastic paraplegia type 57
- Autosomal recessive spastic paraplegia type 5A
- Autosomal recessive spastic paraplegia type 61
- Autosomal recessive spastic paraplegia type 62
- Autosomal recessive spastic paraplegia type 63
- Autosomal recessive spastic paraplegia type 64
- Autosomal recessive spastic paraplegia type 7
- Autosomal recessive spastic paraplegia type 72
- Autosomal recessive spastic paraplegia type 75
- Autosomal recessive spastic paraplegia type 76
- Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type
- Autosomal recessive systemic lupus erythematosus
- Autosomal trisomy
- Autosomal uniparental disomy
- Avascular necrosis
- Avena sativa
- Avulavirus infectious disease
- Aweer
- Axenfeld anomaly
- Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities
- Axenfeld-Rieger syndrome
- Axenfeld-Rieger syndrome type 1
- Axenfeld-Rieger syndrome type 3
- Axial hypotonia
- Axial muscle stiffness
- Axillary freckling
- Axin
