Myhre syndrome
ORPHA:258821q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XX testicular difference of sex development
ORPHA:39347,XYY syndrome
ORPHA:8Acquired generalized lipodystrophy
ORPHA:79086Acropectorovertebral dysplasia
ORPHA:957Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818Androgen insensitivity syndrome
ORPHA:754ANE syndrome
ORPHA:157954Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
ORPHA:1071Anterior maxillary protrusion-strabismus-intellectual disability syndrome
ORPHA:562559Antisynthetase syndrome
ORPHA:81Arthrogryposis-renal dysfunction-cholestasis syndrome
ORPHA:2697Autoimmune interstitial lung disease-arthritis syndrome
ORPHA:444092Autoimmune polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 21
ORPHA:101001Autosomal recessive spastic paraplegia type 23
ORPHA:101003Bannayan-Riley-Ruvalcaba syndrome
ORPHA:109Blepharo-cheilo-odontic syndrome
ORPHA:1997Blepharospasm-oromandibular dystonia syndrome
ORPHA:93964Bohring-Opitz syndrome
ORPHA:97297BOR syndrome
ORPHA:107Brachymorphism-onychodysplasia-dysphalangism syndrome
ORPHA:1292Branchioskeletogenital syndrome
ORPHA:1299C syndrome
ORPHA:1308Cancer-associated retinopathy
ORPHA:71505Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy
ORPHA:199354Choroidal atrophy-alopecia syndrome
ORPHA:1433Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383CLAPO syndrome
ORPHA:168984Cognitive impairment-coarse facies-heart defects-obesity-pulmonary involvement-short stature-skeletal dysplasia syndrome
ORPHA:444077Colobomatous macrophthalmia-microcornea syndrome
ORPHA:468672Congenital contractural arachnodactyly
ORPHA:115Congenital insensitivity to pain syndrome, Marsili type
ORPHA:653728Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome
ORPHA:369861Corneodermatoosseous syndrome
ORPHA:3194Costello syndrome
ORPHA:3071CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-anal anomalies-porokeratosis syndrome
ORPHA:85199