Acrofacial dysostosis, Weyers type
ORPHA:9523C syndrome
ORPHA:73M syndrome
ORPHA:261647,XYY syndrome
ORPHA:8Acrocardiofacial syndrome
ORPHA:2008Acropectorovertebral dysplasia
ORPHA:957Aggressive primary cutaneous T-cell lymphoma
ORPHA:178551Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antiphospholipid syndrome
ORPHA:80Antisynthetase syndrome
ORPHA:81Autoimmune interstitial lung disease-arthritis syndrome
ORPHA:444092Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Blepharo-cheilo-odontic syndrome
ORPHA:1997Bohring-Opitz syndrome
ORPHA:97297Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292C syndrome
ORPHA:1308CACH syndrome
ORPHA:135CAMFAK syndrome
ORPHA:1317CAMOS syndrome
ORPHA:83472Campomelia, Cumming type
ORPHA:1318Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
ORPHA:2848Camptodactyly-tall stature-scoliosis-hearing loss syndrome
ORPHA:85164Cancer-associated retinopathy
ORPHA:71505CANDLE syndrome
ORPHA:325004CANOMAD syndrome
ORPHA:71279Cantú syndrome
ORPHA:1517Cardiofaciocutaneous syndrome
ORPHA:1340Carney complex
ORPHA:1359Caroli syndrome
ORPHA:480520Cataract-hypertrichosis-intellectual disability syndrome
ORPHA:1375Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380CEDNIK syndrome
ORPHA:66631Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
ORPHA:504476Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
ORPHA:1171Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome
ORPHA:603448CHAND syndrome
ORPHA:1401Char syndrome
ORPHA:46627CHARGE syndrome
ORPHA:138CHILD syndrome
ORPHA:139Childhood disintegrative disorder
ORPHA:168782CHIME syndrome
ORPHA:3474Chronic atrial and intestinal dysrhythmia syndrome
ORPHA:435988Chronic Epstein-Barr virus infection syndrome
ORPHA:2566Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CINCA syndrome
ORPHA:1451CK syndrome
ORPHA:251383CLAPO syndrome
ORPHA:168984