Joubert syndrome with oculorenal defect
ORPHA:23182q13 microdeletion syndrome
ORPHA:6847425q22 microdeletion syndrome
ORPHA:261584ABCD syndrome
ORPHA:918Acropectoral syndrome
ORPHA:85203Acropectorovertebral dysplasia
ORPHA:957ADULT syndrome
ORPHA:978Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818ANE syndrome
ORPHA:157954Angelman syndrome
ORPHA:72Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antisynthetase syndrome
ORPHA:81Apert syndrome
ORPHA:87Aplastic anemia-intellectual disability-dwarfism syndrome
ORPHA:611216AREDYLD syndrome
ORPHA:1133Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Asherman syndrome
ORPHA:137686Ataxia-pancytopenia syndrome
ORPHA:2585Autism spectrum disorder due to AUTS2 deficiency
ORPHA:352490Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome
ORPHA:314404Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Banki syndrome
ORPHA:1228Blue rubber bleb nevus
ORPHA:1059C syndrome
ORPHA:1308Cogan syndrome
ORPHA:1467Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome
ORPHA:314002De Barsy syndrome
ORPHA:2962Deficiency in anterior pituitary function-variable immunodeficiency syndrome
ORPHA:293978DEND syndrome
ORPHA:79134Dent disease
ORPHA:1652Denys-Drash syndrome
ORPHA:220Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Dilated cardiomyopathy with ataxia
ORPHA:66634DOORS syndrome
ORPHA:79500Down syndrome
ORPHA:870Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Duane retraction syndrome
ORPHA:233Epilepsy with myoclonic-atonic seizures
ORPHA:1942Familial partial lipodystrophy, Dunnigan type
ORPHA:2348Febrile infection-related epilepsy syndrome
ORPHA:163703Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Frey syndrome
ORPHA:662240H syndrome
ORPHA:168569Helsmoortel-Van der Aa syndrome
ORPHA:404448Holmes-Adie syndrome
ORPHA:454718IMAGe syndrome
ORPHA:85173Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome
ORPHA:513456