46,XX testicular difference of sex development
ORPHA:39321q deletion syndrome
ORPHA:5743C syndrome
ORPHA:73M syndrome
ORPHA:26163MC syndrome
ORPHA:29384346,XY complete gonadal dysgenesis
ORPHA:24247,XYY syndrome
ORPHA:848,XXXY syndrome
ORPHA:9626348,XXYY syndrome
ORPHA:1048,XYYY syndrome
ORPHA:9932949,XXXXY syndrome
ORPHA:9626449,XXXYY syndrome
ORPHA:26153449,XYYYY syndrome
ORPHA:99330Acropectorovertebral 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 polyendocrinopathy type 1
ORPHA:3453Autosomal dominant hyper-IgE syndrome due to STAT3 deficiency
ORPHA:2314Autosomal recessive spastic paraplegia type 21
ORPHA:101001Blepharo-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:1308Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
ORPHA:2848Cancer-associated retinopathy
ORPHA:71505CANDLE syndrome
ORPHA:325004Cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome
ORPHA:228410Cardiofaciocutaneous syndrome
ORPHA:1340Carnevale syndrome
ORPHA:2998Cataract-intellectual disability-hypogonadism syndrome
ORPHA:1387Cataract-nephropathy-encephalopathy syndrome
ORPHA:1380Cerebral autosomal recessive arteriopathy-subcortical infarcts-leukoencephalopathy
ORPHA:199354Cerebrofacioarticular syndrome
ORPHA:314679Choroidal atrophy-alopecia syndrome
ORPHA:1433Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CK syndrome
ORPHA:251383Colobomatous macrophthalmia-microcornea syndrome
ORPHA:468672Complement hyperactivation-angiopathic thrombosis-protein-losing enteropathy syndrome
ORPHA:566175Congenital contractural arachnodactyly
ORPHA:115Congenital insensitivity to pain syndrome, Marsili type
ORPHA:653728