OBSOLETE: Mandibulofacial dysostosis-deafness-postaxial polydactyly syndrome
ORPHA:2458OBSOLETE: Amniotic bands
ORPHA:1034OBSOLETE: ATR-X-related syndrome
ORPHA:263355OBSOLETE: Autosomal dominant Opitz G/BBB syndrome
ORPHA:306588OBSOLETE: Cranioacrofacial syndrome
ORPHA:1339OBSOLETE: Craniosynostosis-fibular aplasia syndrome
ORPHA:1533OBSOLETE: Cushing syndrome
ORPHA:553OBSOLETE: Ectodermal dysplasia-absent dermatoglyphs syndrome
ORPHA:1235OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
ORPHA:2129OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
ORPHA:3050OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome
ORPHA:3313OBSOLETE: Ito hypomelanosis
ORPHA:435OBSOLETE: Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome
ORPHA:2005OBSOLETE: Lown-Ganong-Levine syndrome
ORPHA:844OBSOLETE: Oculo-skeletal-renal syndrome
ORPHA:2716OBSOLETE: Oculocerebroosseous syndrome
ORPHA:2708OBSOLETE: Orofaciodigital syndrome type 10
ORPHA:2756OBSOLETE: Orofaciodigital syndrome type 13
ORPHA:141330OBSOLETE: Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome
ORPHA:2787OBSOLETE: Paraplegia-brachydactyly-cone-shaped epiphysis syndrome
ORPHA:2823OBSOLETE: Pilotto syndrome
ORPHA:2894OBSOLETE: Sakati-Nyhan syndrome
ORPHA:3128OBSOLETE: Say-Field-Coldwell syndrome
ORPHA:3133OBSOLETE: Short stature-microcephaly-heart defect syndrome
ORPHA:2861OBSOLETE: Shy-Drager syndrome
ORPHA:98932OBSOLETE: Spastic diplegia, infantile type
ORPHA:1680OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome
ORPHA:3362OBSOLETE: X-linked Opitz G/BBB syndrome
ORPHA:306597Reynolds syndrome
ORPHA:779