Generalized eruptive keratoacanthoma
ORPHA:41177721q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384347,XYY syndrome
ORPHA:8Acrogeria
ORPHA:2500Acropectoral syndrome
ORPHA:85203Acropectorovertebral dysplasia
ORPHA:957Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune interstitial lung disease-arthritis syndrome
ORPHA:444092Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 21
ORPHA:101001Aymé-Gripp syndrome
ORPHA:1272B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502Banki syndrome
ORPHA:1228Behr syndrome
ORPHA:1239BIDS syndrome
ORPHA:1245Biliary atresia with splenic malformation syndrome
ORPHA:244283Blau syndrome
ORPHA:90340Blepharo-cheilo-odontic syndrome
ORPHA:1997Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Bowen syndrome
ORPHA:1271Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Cancer-associated retinopathy
ORPHA:71505Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
ORPHA:504476Char syndrome
ORPHA:46627Childhood-onset basal ganglia degeneration syndrome
ORPHA:497906Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CNTNAP2-related developmental and epileptic encephalopathy
ORPHA:163681Congenital contractural arachnodactyly
ORPHA:115Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194