Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Down syndrome
ORPHA:870Ectrodactyly-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:412022Familial 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:595216Filippi 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:93256Fraser syndrome
ORPHA:2052Frasier syndrome
ORPHA:347FRAXF syndrome
ORPHA:100974Frey syndrome
ORPHA:662240Fried syndrome
ORPHA:85335Fryns syndrome
ORPHA:2059Furlong syndrome
ORPHA:97295GAPO 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:306741HNF1B-related autosomal dominant tubulointerstitial kidney disease
ORPHA:93111Holmes-Adie syndrome
ORPHA:454718Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882