OBSOLETE: Orofaciodigital syndrome type 12
ORPHA:141327Familial atypical multiple mole melanoma syndrome
ORPHA:404560MORM syndrome
ORPHA:75858Morvan syndrome
ORPHA:83467OBSOLETE: ACTH-independent Cushing syndrome
ORPHA:99893OBSOLETE: Adult-onset SAPHO syndrome
ORPHA:324982OBSOLETE: Amniotic bands
ORPHA:1034OBSOLETE: Antenatal Bartter syndrome
ORPHA:93604OBSOLETE: ATR-X-related syndrome
ORPHA:263355OBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactyly
ORPHA:3357OBSOLETE: AymÚ-Gripp syndrome
ORPHA:477668OBSOLETE: Benign exophthalmos syndrome
ORPHA:71269OBSOLETE: Blaichman syndrome
ORPHA:1250OBSOLETE: Blepharophimosis-radioulnar synostosis syndrome
ORPHA:1256OBSOLETE: Bowed tibiae-radial anomalies-osteopenia-fractures syndrome
ORPHA:3331OBSOLETE: Cardioskeletal syndrome
ORPHA:98734OBSOLETE: Cataract-intellectual disability-anal atresia-urinary defects syndrome
ORPHA:1381OBSOLETE: Cerebrofacial arteriovenous metameric syndrome type 2
ORPHA:53719OBSOLETE: Cerebrorenodigital syndrome
ORPHA:1396OBSOLETE: Corpus callosum agenesis-double urinary collecting system-trigonocephaly syndrome
ORPHA:1492OBSOLETE: Cranioacrofacial syndrome
ORPHA:1339OBSOLETE: Craniofaciocervical osteoglyphic dysplasia
ORPHA:1800OBSOLETE: Craniosynostosis-fibular aplasia syndrome
ORPHA:1533OBSOLETE: Craniosynostosis-radial aplasia, Imaizumi type
ORPHA:1534OBSOLETE: Craniosynostosis-synostoses-hypertensive nephropathy syndrome
ORPHA:1526OBSOLETE: Cushing syndrome
ORPHA:553OBSOLETE: Dacryocystitis-osteopoikilosis syndrome
ORPHA:1562OBSOLETE: Deafness-white hair-contractures-papillomas syndrome
ORPHA:3215OBSOLETE: Dennis-Cohen syndrome
ORPHA:1651OBSOLETE: Dwarfism-intellectual disability-eye abnormality syndrome
ORPHA:2650OBSOLETE: Ectodermal dysplasia-absent dermatoglyphs syndrome
ORPHA:1235OBSOLETE: Familial intestinal malrotation-facial anomalies syndrome
ORPHA:2454OBSOLETE: Foix-Alajouanine syndrome
ORPHA:79093OBSOLETE: Hashimoto-Pritzker syndrome
ORPHA:99872OBSOLETE: Heckenlively syndrome
ORPHA:2120OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
ORPHA:2129OBSOLETE: Hypopituitarism-short stature-skeletal anomalies syndrome
ORPHA:2626OBSOLETE: Ichthyosis-cheek-eyebrow syndrome
ORPHA:2267OBSOLETE: Infantile epilepsy syndrome
ORPHA:98258OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome
ORPHA:3050OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome
ORPHA:3313OBSOLETE: Intellectual disability-unusual facies syndrome
ORPHA:3043OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type
ORPHA:3046OBSOLETE: Ito hypomelanosis
ORPHA:435OBSOLETE: Juvenile-onset SAPHO syndrome
ORPHA:324989OBSOLETE: Laryngo-tracheo-esophageal cleft-pulmonary hypoplasia syndrome
ORPHA:2005OBSOLETE: Lethal chondrodysplasia, Moerman type
ORPHA:1420OBSOLETE: Low birth weight-dwarfism-dysgammaglobulinemia syndrome
ORPHA:2621