Pseudohypoparathyroidism type 1A
ORPHA:79443Pudendal nerve entrapment syndrome
ORPHA:60039Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
ORPHA:71289Right isomerism
ORPHA:97548Ring chromosome 1 syndrome
ORPHA:1437Ring chromosome 4 syndrome
ORPHA:1447Ring chromosome 8 syndrome
ORPHA:1450Sanjad-Sakati syndrome
ORPHA:2323Seizures-scoliosis-macrocephaly syndrome
ORPHA:466926Semicircular canal dehiscence syndrome
ORPHA:420402Severe dermatitis-multiple allergies-metabolic wasting syndrome
ORPHA:369992Severe oculo-renal-cerebellar syndrome
ORPHA:2715Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome
ORPHA:397623Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
ORPHA:314394Short stature-optic atrophy-Pelger-Huët anomaly syndrome
ORPHA:391677Silent sinus syndrome
ORPHA:71276Smith-Lemli-Opitz syndrome
ORPHA:818Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome
ORPHA:521390Syndactyly-telecanthus-anogenital and renal malformations syndrome
ORPHA:140952Thrombocytopenia-absent radius syndrome
ORPHA:3320Tricho-dento-osseous syndrome
ORPHA:3352Triple A syndrome
ORPHA:869Trisomy X syndrome
ORPHA:3375W syndrome
ORPHA:2804Wolf-Hirschhorn syndrome
ORPHA:280X-linked alpha-thalassemia-intellectual disability syndrome
ORPHA:847X-linked intellectual disability-retinitis pigmentosa syndrome
ORPHA:85332X-linked intellectual disability-spastic paraplegia with iron deposits syndrome
ORPHA:85333XK aprosencephaly syndrome
ORPHA:3469Xq21 microdeletion syndrome
ORPHA:1435