Isolated anterior cervical hypertrichosis
ORPHA:338722q11.2 deletion syndrome
ORPHA:5673C syndrome
ORPHA:73M syndrome
ORPHA:2616Absence of fingerprints-congenital milia syndrome
ORPHA:1658Acrofacial dysostosis, Weyers type
ORPHA:952Acropectorovertebral dysplasia
ORPHA:957Aggressive primary cutaneous T-cell lymphoma
ORPHA:178551Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Antiphospholipid syndrome
ORPHA:80Antisynthetase syndrome
ORPHA:81Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal recessive spastic paraplegia type 20
ORPHA:101000BIDS syndrome
ORPHA:1245C syndrome
ORPHA:1308Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Childhood disintegrative disorder
ORPHA:168782CK syndrome
ORPHA:251383Congenital heart defect-ectodermal dysplasia- brachydactyly-telangiectasia syndrome
ORPHA:708019Corneal dystrophy-perceptive deafness syndrome
ORPHA:1490De Hauwere syndrome
ORPHA:1831Diaphyseal medullary stenosis-bone malignancy syndrome
ORPHA:85182Distal deletion 3p syndrome
ORPHA:1620Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Encephalocraniocutaneous lipomatosis
ORPHA:2396Facial dysmorphism-ocular anomalies-osteopenia-intellectual disability-dental anomalies syndrome
ORPHA:314555Frank-Ter Haar syndrome
ORPHA:137834Fryns-Smeets-Thiry syndrome
ORPHA:2058H syndrome
ORPHA:168569Haddad syndrome
ORPHA:99803Haim-Munk syndrome
ORPHA:2342Hall-Riggs syndrome
ORPHA:2107HANAC syndrome
ORPHA:73229Hardikar syndrome
ORPHA:1415Harlequin syndrome
ORPHA:199282HARP syndrome
ORPHA:157855Harrod syndrome
ORPHA:2115Hartsfield syndrome
ORPHA:2117Heart-hand syndrome
ORPHA:228184HEC syndrome
ORPHA:2119Heiner syndrome
ORPHA:99932HELLP syndrome
ORPHA:244242Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hemiparkinsonism-hemiatrophy syndrome
ORPHA:306669Hereditary acrokeratotic poikiloderma
ORPHA:2907HERNS syndrome
ORPHA:63261HIDEA syndrome
ORPHA:436141