OBSOLETE: Ehlers-Danlos syndrome, fibronectinemic type
ORPHA:75501Arthrochalasia Ehlers-Danlos syndrome
ORPHA:1899B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome
ORPHA:536467Brittle cornea syndrome
ORPHA:90354Cardiac-valvular Ehlers-Danlos syndrome
ORPHA:230851Classical Ehlers-Danlos syndrome
ORPHA:287Classical-like Ehlers-Danlos syndrome type 1
ORPHA:230839Classical-like Ehlers-Danlos syndrome type 2
ORPHA:536532Dermatosparaxis Ehlers-Danlos syndrome
ORPHA:1901Ehlers-Danlos syndrome
ORPHA:98249Ehlers-Danlos/osteogenesis imperfecta syndrome
ORPHA:230857Feingold syndrome type 1
ORPHA:391641Hypermobile Ehlers-Danlos syndrome
ORPHA:285Kyphoscoliotic Ehlers-Danlos syndrome
ORPHA:536545Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency
ORPHA:1900Musculocontractural Ehlers-Danlos syndrome
ORPHA:2953Myopathic Ehlers-Danlos syndrome
ORPHA:536516OBSOLETE: Amniotic bands
ORPHA:1034OBSOLETE: Antenatal Bartter syndrome
ORPHA:93604OBSOLETE: Autosomal recessive hyper-IgE syndrome
ORPHA:169446OBSOLETE: AymÚ-Gripp syndrome
ORPHA:477668OBSOLETE: Blaichman syndrome
ORPHA:1250OBSOLETE: Cranioacrofacial syndrome
ORPHA:1339OBSOLETE: Craniosynostosis-fibular aplasia syndrome
ORPHA:1533OBSOLETE: Cushing syndrome
ORPHA:553OBSOLETE: Deafness-white hair-contractures-papillomas syndrome
ORPHA:3215OBSOLETE: Dennis-Cohen syndrome
ORPHA:1651OBSOLETE: Ectodermal dysplasia-absent dermatoglyphs syndrome
ORPHA:1235OBSOLETE: Ehlers-Danlos syndrome type 1
ORPHA:90309OBSOLETE: Ehlers-Danlos syndrome type 2
ORPHA:90318OBSOLETE: Ehlers-Danlos syndrome type 7A
ORPHA:99875OBSOLETE: Ehlers-Danlos syndrome type 7B
ORPHA:99876OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
ORPHA:2129OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
ORPHA:3050OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome
ORPHA:3313OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type
ORPHA:3046OBSOLETE: Ito hypomelanosis
ORPHA:435OBSOLETE: Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome
ORPHA:2005OBSOLETE: Lown-Ganong-Levine syndrome
ORPHA:844OBSOLETE: McLain-Dekaban syndrome
ORPHA:2474OBSOLETE: MECP2 duplication syndrome
ORPHA:85281OBSOLETE: Mickleson syndrome
ORPHA:2507OBSOLETE: Oculocerebroosseous syndrome
ORPHA:2708OBSOLETE: Orofaciodigital syndrome type 10
ORPHA:2756OBSOLETE: Orofaciodigital syndrome type 12
ORPHA:141327OBSOLETE: Orofaciodigital syndrome type 13
ORPHA:141330OBSOLETE: Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome
ORPHA:2787OBSOLETE: Peeling skin syndrome type C
ORPHA:263558