Transient familial neonatal hyperbilirubinemia
ORPHA:2312Autosomal dominant deafness-onychodystrophy syndrome
ORPHA:79499Blue diaper syndrome
ORPHA:94086Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024DEND 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:870Dravet syndrome
ORPHA:33069Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Febrile infection-related epilepsy syndrome
ORPHA:163703Frey syndrome
ORPHA:662240Hypergonadotropic hypogonadism-cataract syndrome
ORPHA:2410L1 syndrome
ORPHA:275543Lacrimoauriculodentodigital syndrome
ORPHA:2363Laryngo-onycho-cutaneous syndrome
ORPHA:2407LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369LUMBAR syndrome
ORPHA:83628Mohr-Tranebjaerg syndrome
ORPHA:52368Null syndrome
ORPHA:280234Oculocerebrorenal syndrome of Lowe
ORPHA:534Oley syndrome
ORPHA:79458Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome
ORPHA:2928Scott syndrome
ORPHA:806Toxic epidermal necrolysis
ORPHA:537X-linked dystonia-parkinsonism
ORPHA:53351