eRAM

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

About 15942 Results.

501	perrault syndrome
502	klatskin tumor
503	thymic carcinoma
504	scrub typhus
505	opsismodysplasia
506	bruck syndrome
507	schnitzler syndrome
508	hypopituitarism
509	monilethrix
510	infantile myofibromatosis
511	thymoma
512	tarsal-carpal coalition syndrome
513	placental site trophoblastic tumor
514	acrodermatitis enteropathica
515	lysinuric protein intolerance
516	severe acute respiratory syndrome
517	laurence-moon syndrome
518	hypochondroplasia
519	pustulosis palmaris et plantaris
520	megalencephaly
521	cutaneous lupus erythematosus
522	nance-horan syndrome
523	ichthyosis
524	blau syndrome
525	early myoclonic encephalopathy
526	adenine phosphoribosyltransferase deficiency
527	chylomicron retention disease
528	hairy cell leukemia
529	larsen syndrome
530	familial partial lipodystrophy
531	purine nucleoside phosphorylase deficiency
532	thalassemia
533	hepatic veno-occlusive disease
534	cat-scratch disease
535	timothy syndrome
536	infantile neuroaxonal dystrophy
537	cardiofaciocutaneous syndrome
538	juvenile xanthogranuloma
539	lyme disease
540	keratoconus
541	hypereosinophilic syndrome
542	adamantinoma
543	poliomyelitis
544	autoimmune hemolytic anemia
545	brucellosis
546	hyperparathyroidism
547	cornelia de lange syndrome
548	endocardial fibroelastosis
549	hydrocephalus
550	dyschromatosis symmetrica hereditaria
551	1p36 deletion syndrome
552	desmoid tumor
553	thrombocytopenia
554	leptospirosis
555	mandibuloacral dysplasia
556	graft versus host disease
557	congenital fiber type disproportion
558	nelson syndrome
559	primary hyperparathyroidism
560	distal myopathy
561	apraxia
562	cardiomyopathy
563	post polio syndrome
564	meconium aspiration syndrome
565	3m syndrome
566	meesmann corneal dystrophy
567	spondylometaphyseal dysplasia
568	best vitelliform macular dystrophy
569	multiple sulfatase deficiency
570	situs ambiguus
571	white sponge nevus
572	antithrombin deficiency
573	salla disease
574	microphthalmia
575	hereditary multiple exostoses
576	tyrosinemia type 1
577	lysosomal acid lipase deficiency
578	ichthyosis linearis circumflexa
579	mast cell sarcoma
580	pallister hall syndrome
581	holt oram syndrome
582	russell silver syndrome
583	hermansky pudlak syndrome
584	smith magenis syndrome
585	wolf hirschhorn syndrome
586	smallpox
587	thrombophilia
588	neutropenia
589	pemphigus
590	hepatitis c
591	pancreatitis
592	intracranial aneurysm
593	glomerulonephritis
594	periodontitis
595	anthrax
596	gallbladder cancer
597	common variable immune deficiency
598	neuralgic amyotrophy
599	hyperprolactinemia
600	factor x deficiency

Rare Disease
Scleroderma ;
Biotinidase deficiency ;
Coats disease ;
Cyclic neutropenia ;
Cystinuria