OBSOLETE: Oculocerebroacral syndrome
ORPHA:2706OBSOLETE: 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: Otopalatodigital syndrome
ORPHA:669OBSOLETE: Partial prune belly syndrome
ORPHA:93178OBSOLETE: Pediatric Sjögren syndrome
ORPHA:93566OBSOLETE: Peeling skin syndrome type C
ORPHA:263558OBSOLETE: Peters anomaly-cataract syndrome
ORPHA:101033OBSOLETE: Pilotto syndrome
ORPHA:2894OBSOLETE: Pitt-Hopkins-like syndrome
ORPHA:221150OBSOLETE: Pulmonary aortic stenosis obstructive uropathy
ORPHA:1137OBSOLETE: Ramsay Hunt syndrome type II
ORPHA:412220OBSOLETE: Sakati-Nyhan syndrome
ORPHA:3128OBSOLETE: Say-Field-Coldwell syndrome
ORPHA:3133OBSOLETE: Short stature-heart defect-craniofacial anomalies syndrome
ORPHA:1088OBSOLETE: Short stature-microcephaly-heart defect syndrome
ORPHA:2861OBSOLETE: Shy-Drager syndrome
ORPHA:98932OBSOLETE: Spastic diplegia, infantile type
ORPHA:1680OBSOLETE: Sporadic Leigh syndrome
ORPHA:255199OBSOLETE: Syndromic frontonasal dysplasia
ORPHA:391479OBSOLETE: Syndromic myopia
ORPHA:98620OBSOLETE: Taussig-Bing syndrome
ORPHA:101042OBSOLETE: Torres-Aybar syndrome
ORPHA:3340OBSOLETE: Tricho-oculo-dermo-vertebral syndrome
ORPHA:3354OBSOLETE: Trichomegaly-cataract-hereditary spherocytosis syndrome
ORPHA:3362OBSOLETE: Van den Bosch syndrome
ORPHA:3417OBSOLETE: X-linked Opitz G/BBB syndrome
ORPHA:306597OBSOLETE: Zlotogura-Martinez syndrome
ORPHA:101036