Birth Defects - Syndromes - Malformations - Anomalies
- S
- Schereshevskij
- Schereshevskij Turner
- Schmid Fraccaro
- Schwannomatosis
- Scleroderma (in children)
- Scoliosis in general
- Scoliosis as part of NF
- Scott Aarskog
- SEDc
- Seemanova II
- Segmental Neurofibromatosis
- Seizures
- Selenium
- SEMD Strudwick Type
- Sequence Cloacal
- Sex Diffrentiation
- Sex Reversal, Autosomal, 1
- Short Limb Dwarfism Peters Anomaly
- Short Stature
- Shprintzen Omphalocele
- Shprintzen VCF
- Sífilis Congénita
- Silver-Russell Syndrome
- Sipple
- Sindrome = vea mombres
- Skeletal Dysplasia
- SMED Strudwick Type
- SMED Type 1
- Soriatane (actiretin)
- SOX9
- Spina Bifida
- Spinal Cords (Tethered)
- Splanchnica Exstrophia
- Spondyloepiphyseal Dysplasia Congenita
- Spondyloepimetaphyseal Dysplasia Strudwick
- Spurway-Eddowes
- SRY-BOX 9
- SRY-Related HMG-BOX GENE 9
- Steroid 11 - Beta - Hydroxylase
- Steroid Cytochrome P450 21-Hydroxylase
- Stickler - Marshall
- Stickler, Type I
- Stickler, Type II
- Stickler, Type III
- Streeter's (Amniotic Bands)
- Strudwick
- Sturge Weber Dimitri
- Stuttering
- Sugio Kagii
- Surveillance
- Syndrome = see eponyms
- Synkinesia Bimanual
- Systemic Sclerosis
