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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



  Precise Disease Search  
Please enter a rare disease name and press Search, then you will gain the related annotation of the certain rare disease.

  Fuzzy Disease Search
Please enter a likely rare disease name (more than 2 characters) and press Search, then you will gain the related annotation of the likely rare disease.

  The First 2000 Rare Disease
About 15942 Results.
  ID Disease
  401 smith lemli opitz syndrome
  402 dystonia
  403 sick sinus syndrome
  404 narcolepsy
  405 uveitis
  406 meningioma
  407 nephrotic syndrome
  408 antiphospholipid syndrome
  409 hypothyroidism
  410 hypertrophic cardiomyopathy
  411 bronchopulmonary dysplasia
  412 autoimmune hepatitis
  413 myalgic encephalomyelitis
  414 premature ovarian failure
  415 thoracic aortic aneurysm
  416 pilomatrixoma
  417 nail-patella syndrome
  418 temporal arteritis
  419 muckle-wells syndrome
  420 charcot-marie-tooth disease
  421 localized scleroderma
  422 hydatidiform mole
  423 diffuse cutaneous systemic sclerosis
  424 becker muscular dystrophy
  425 cartilage-hair hypoplasia
  426 panhypopituitarism
  427 peters anomaly
  428 west syndrome
  429 brittle cornea syndrome
  430 cutaneous mastocytoma
  431 balkan nephropathy
  432 schistosomiasis
  433 mowat-wilson syndrome
  434 langer-giedion syndrome
  435 factor xii deficiency
  436 cadasil
  437 ewing sarcoma
  438 machado-joseph disease
  439 arrhythmogenic right ventricular cardiomyopathy
  440 metabolic syndrome x
  441 chronic myeloproliferative disease
  442 nemaline myopathy
  443 basal cell nevus syndrome
  444 charcot-marie-tooth disease type 1a
  445 familial benign chronic pemphigus
  446 systemic mastocytosis
  447 porphyria variegata
  448 buerger disease
  449 clear cell renal carcinoma
  450 isolated polycystic liver disease
  451 berardinelli-seip congenital lipodystrophy
  452 crouzon disease
  453 merrf
  454 fructose intolerance
  455 multiple acyl-coa dehydrogenase deficiency
  456 monoclonal gammopathy of uncertain significance
  457 congenital lymphedema
  458 sjogren's syndrome
  459 acute lymphocytic leukemia
  460 sclerosing cholangitis
  461 b-cell lymphomas
  462 vesicoureteral reflux
  463 astrocytoma
  464 microscopic polyangiitis
  465 kniest dysplasia
  466 gray platelet syndrome
  467 cockayne syndrome
  468 hemolytic-uremic syndrome
  469 acanthosis nigricans
  470 double outlet right ventricle
  471 porokeratosis
  472 lissencephaly
  473 achromatopsia
  474 klinefelter syndrome
  475 scleroderma
  476 hepatoblastoma
  477 boomerang dysplasia
  478 microcephaly
  479 paroxysmal nocturnal hemoglobinuria
  480 cushing syndrome
  481 rhabdomyosarcoma
  482 rapadilino syndrome
  483 piebaldism
  484 felty syndrome
  485 angioimmunoblastic t-cell lymphoma
  486 fibrochondrogenesis
  487 pyomyositis
  488 aspartylglucosaminuria
  489 pulmonary arterial hypertension
  490 congenital dyserythropoietic anemia
  491 waardenburg syndrome
  492 tardive dyskinesia
  493 myositis
  494 cogan syndrome
  495 complete androgen insensitivity syndrome
  496 cerebral amyloid angiopathy
  497 evans syndrome
  498 fucosidosis
  499 cohen syndrome
  500 anencephaly

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