CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199Curly hair-acral keratoderma-caries syndrome
ORPHA:307766Deafness with labyrinthine aplasia, microtia, and microdontia
ORPHA:90024Dent disease
ORPHA:1652Diethylstilbestrol syndrome
ORPHA:1916Digitorenocerebral syndrome
ORPHA:1674Distal deletion 3p syndrome
ORPHA:1620Donnai-Barrow syndrome
ORPHA:2143DOORS syndrome
ORPHA:79500Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411EAST syndrome
ORPHA:199343Ectrodactyly-cleft palate syndrome
ORPHA:1889EEC syndrome
ORPHA:1896EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Erythrokeratodermia-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:595216FLOTCH syndrome
ORPHA:2045Foveal 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:93256Fraser syndrome
ORPHA:2052Frey syndrome
ORPHA:662240Fried syndrome
ORPHA:85335Fryns syndrome
ORPHA:2059GAPO syndrome
ORPHA:2067GMS syndrome
ORPHA:2090Gorlin-Chaudhry-Moss syndrome
ORPHA:2095Growth deficiency-brachydactyly-dysmorphism syndrome
ORPHA:2055H syndrome
ORPHA:168569HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741