Experimental Factor Ontology
832 terms(s) returned
| Term Type: | Record: 1 to 50 of 832 Records | Page: 1 of 17, First Previous Next Last | Show Records Per Page |
- SATB2 associated disorder
- SCARF syndrome
- SCN4A-related channelopathy
- SCN4A-related myopathy, autosomal recessive
- SEC61A1 deficiency
- SELENON-related myopathy
- SERAC1-related neurological disorder
- SERKAL syndrome
- SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth
- SF3B4-related acrofacial dysostosis
- SHORT syndrome
- SHOX-related short stature
- SIM1-related Prader-Willi-like syndrome
- SIN3A-related intellectual disability syndrome
- SLC35A1-congenital disorder of glycosylation
- SLC35A2-congenital disorder of glycosylation
- SLC39A8-CDG
- SLC6A3-related dopamine transporter deficiency syndrome
- SMARCB1-deficient kidney medullary carcinoma
- SMARCC1-associated developmental dysgenesis syndrome
- SPAST-related motor disorder
- SRD5A3-congenital disorder of glycosylation
- SSR4-congenital disorder of glycosylation
- STING-associated vasculopathy with onset in infancy
- STT3A-congenital disorder of glycosylation
- STT3B-congenital disorder of glycosylation
- SYNCRIP-related neurodevelopmental disorder
- SYNGAP1-related developmental and epileptic encephalopathy
- Saethre-Chotzen syndrome
- Sakati-Nyhan syndrome
- Salla disease
- Sandhoff disease
- Sandhoff disease, adult form
- Sandhoff disease, infantile form
- Sandhoff disease, juvenile form
- Say-Barber-Miller syndrome
- Say-field-Coldwell syndrome
- SchC6pf-Schulz-Passarge syndrome
- Schaaf-Yang syndrome
- Scheie syndrome
- Scheuermann disease
- Schilbach-Rott syndrome
- Schimke immuno-osseous dysplasia
- Schinzel-Giedion syndrome
- Schmid metaphyseal chondrodysplasia
- Schnyder corneal dystrophy
- Schuurs-Hoeijmakers syndrome
- Schwartz-Jampel syndrome
- Scott syndrome
- Seckel syndrome
