Bartter syndrome type 1
ORPHA:620217Bartter syndrome type 2
ORPHA:620220Bartter syndrome type 3
ORPHA:93605Bartter syndrome type 4
ORPHA:8993846,XY complete gonadal dysgenesis
ORPHA:242Aase-Smith syndrome type 1
ORPHA:916Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acquired partial lipodystrophy
ORPHA:79087ALG1-CDG
ORPHA:79327ALG11-CDG
ORPHA:280071ALG12-CDG
ORPHA:79324ALG13-CDG
ORPHA:324422ALG2-CDG
ORPHA:79326ALG3-CDG
ORPHA:79321ALG6-CDG
ORPHA:79320ALG8-CDG
ORPHA:79325ALG9-CDG
ORPHA:79328Alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
ORPHA:98791Andersen-Tawil syndrome
ORPHA:37553Arthrochalasia Ehlers-Danlos syndrome
ORPHA:1899Ataxia-telangiectasia
ORPHA:100Autosomal dominant otospondylomegaepiphyseal dysplasia
ORPHA:166100Autosomal recessive spastic paraplegia type 20
ORPHA:101000B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome
ORPHA:567502B4GALT1-CDG
ORPHA:79332Balint syndrome
ORPHA:363746Ballard syndrome
ORPHA:93395Bamforth-Lazarus syndrome
ORPHA:1226Bangstad syndrome
ORPHA:1227Banki syndrome
ORPHA:1228Barber-Say syndrome
ORPHA:1231Bardet-Biedl syndrome
ORPHA:110Barth syndrome
ORPHA:111Bartsocas-Papas syndrome
ORPHA:1234Bartter syndrome
ORPHA:112Bartter syndrome with hypocalcemia
ORPHA:263417Bazex syndrome
ORPHA:166113Behr syndrome
ORPHA:1239BIDS syndrome
ORPHA:1245Biemond syndrome type 2
ORPHA:141333Biliary atresia with splenic malformation syndrome
ORPHA:244283Birk-Barel syndrome
ORPHA:166108Blau syndrome
ORPHA:90340Blepharo-cheilo-odontic syndrome
ORPHA:1997Blue rubber bleb nevus
ORPHA:1059BNAR syndrome
ORPHA:217266Bohring-Opitz syndrome
ORPHA:97297Böök syndrome
ORPHA:1262