OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
ORPHA:2129Acropectorovertebral dysplasia
ORPHA:957Autoimmune polyendocrinopathy type 1
ORPHA:3453Blepharophimosis-intellectual disability syndrome, Ohdo type
ORPHA:2728C syndrome
ORPHA:1308Carnevale syndrome
ORPHA:2998Chronic intestinal pseudoobstruction syndrome
ORPHA:2978CLAPO syndrome
ORPHA:168984Double uterus-hemivagina-renal agenesis syndrome
ORPHA:3411Feingold syndrome
ORPHA:1305GAPO syndrome
ORPHA:2067H syndrome
ORPHA:168569HANAC syndrome
ORPHA:73229HARP syndrome
ORPHA:157855HEC syndrome
ORPHA:2119HELLP syndrome
ORPHA:244242Hemiconvulsion-hemiplegia-epilepsy syndrome
ORPHA:86908Hemidystonia-hemiatrophy syndrome
ORPHA:306741Hemiparkinsonism-hemiatrophy syndrome
ORPHA:306669HERNS syndrome
ORPHA:63261HIDEA syndrome
ORPHA:436141Hinman syndrome
ORPHA:84085Holt-Oram syndrome
ORPHA:392Hyperinsulinism-hyperammonemia syndrome
ORPHA:35878Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome
ORPHA:415Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome
ORPHA:363694Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome
ORPHA:528105Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936Infantile-onset spinocerebellar ataxia
ORPHA:1186KID syndrome
ORPHA:477N syndrome
ORPHA:2608OBSOLETE: ACTH-independent Cushing syndrome
ORPHA:99893OBSOLETE: Adult-onset SAPHO syndrome
ORPHA:324982OBSOLETE: Amniotic bands
ORPHA:1034OBSOLETE: Angioosteohypertrophic syndrome
ORPHA:2346OBSOLETE: Antenatal Bartter syndrome
ORPHA:93604OBSOLETE: ATR-X-related syndrome
ORPHA:263355OBSOLETE: Autosomal dominant Opitz G/BBB syndrome
ORPHA:306588OBSOLETE: Autosomal dominant spastic paraplegia type 9
ORPHA:100990OBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactyly
ORPHA:3357OBSOLETE: Autosomal recessive hyper-IgE syndrome
ORPHA:169446OBSOLETE: AymÚ-Gripp syndrome
ORPHA:477668OBSOLETE: Benign exophthalmos syndrome
ORPHA:71269OBSOLETE: Blaichman syndrome
ORPHA:1250OBSOLETE: Blepharophimosis-radioulnar synostosis syndrome
ORPHA:1256