Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Deficiency 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:66634Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
ORPHA:2229Distal deletion 3p syndrome
ORPHA:1620Dobrow syndrome
ORPHA:3262Donohue syndrome
ORPHA:508DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870Dravet syndrome
ORPHA:33069Drug reaction with eosinophilia and systemic symptoms
ORPHA:139402Duane retraction syndrome
ORPHA:233Dursun syndrome
ORPHA:178503DYRK1A-related intellectual disability syndrome
ORPHA:464306Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Epilepsy with myoclonic-atonic seizures
ORPHA:1942Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome
ORPHA:1969Facial dysmorphism-hypertrichosis-epilepsy-intellectual disability/developmental delay-gingival overgrowth syndrome
ORPHA:598603Facial dysmorphism-immunodeficiency-livedo-short stature syndrome
ORPHA:352712Facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome
ORPHA:412022Facial onset sensory and motor neuronopathy
ORPHA:85162Familial atypical multiple mole melanoma syndrome
ORPHA:404560FATCO syndrome
ORPHA:2492Febrile infection-related epilepsy syndrome
ORPHA:163703Feingold syndrome
ORPHA:1305Felty syndrome
ORPHA:47612Fibrous dysplasia/McCune-Albright syndrome
ORPHA:595216Fibular aplasia-complex brachydactyly syndrome
ORPHA:2639Filippi syndrome
ORPHA:3255FLOTCH syndrome
ORPHA:2045Fountain syndrome
ORPHA:3219Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
ORPHA:397618Fowler urethral sphincter dysfunction syndrome
ORPHA:2795FOXG1 syndrome
ORPHA:561854FOXP1 Syndrome
ORPHA:391372Fragile X syndrome
ORPHA:908Fragile X-associated tremor/ataxia syndrome
ORPHA:93256