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.

601	scheuermann disease
602	agammaglobulinemia
603	factor v deficiency
604	familial melanoma
605	mosaic variegated aneuploidy syndrome
606	cranioectodermal dysplasia
607	trisomy 18
608	cutaneous mastocytosis
609	mccune-albright syndrome
610	bannayan-riley-ruvalcaba syndrome
611	leopard syndrome
612	tyrosinemia
613	pyle disease
614	duane retraction syndrome
615	indolent systemic mastocytosis
616	usher syndrome type 1
617	lennox-gastaut syndrome
618	factor vii deficiency
619	anthracosis
620	niemann-pick disease type a
621	kartagener syndrome
622	diffuse large b-cell lymphoma
623	waldenstrom macroglobulinemia
624	malignant peritoneal mesothelioma
625	allan-herndon-dudley syndrome
626	renal tubular acidosis
627	hallermann-streiff syndrome
628	familial periodic paralysis
629	birt-hogg-dube syndrome
630	ebola hemorrhagic fever
631	acoustic neuroma
632	medullary thyroid carcinoma
633	bor syndrome
634	cerebral cavernous malformations
635	triple a syndrome
636	congenital erythropoietic porphyria
637	american trypanosomiasis
638	mucolipidosis iv
639	benign schwannoma
640	neural tube defects
641	open-angle glaucoma
642	dental ankylosis
643	soft tissue sarcoma
644	erythroderma desquamativum
645	gyrate atrophy of choroid and retina
646	periarteritis nodosa
647	congenital nonhemolytic jaundice
648	hereditary hyperuricemia
649	duodenal ulcer
650	basal cell carcinoma
651	membranous nephropathy
652	usher syndrome type 3
653	angioosteohypertrophic syndrome
654	arteritis, takayasu
655	dystrophy, myotonic
656	fibrosarcoma
657	fascioliasis
658	truncus arteriosus
659	short syndrome
660	multiple carboxylase deficiency
661	carcinoid syndrome
662	necrotizing enterocolitis
663	oligodendroglioma
664	pityriasis rosea
665	infant botulism
666	amelogenesis imperfecta
667	dense deposit disease
668	listeriosis
669	liposarcoma
670	medullary sponge kidney
671	melorheostosis
672	erythema elevatum diutinum
673	axenfeld-rieger syndrome
674	taurodontism
675	neonatal adrenoleukodystrophy
676	alternating hemiplegia of childhood
677	paroxysmal extreme pain disorder
678	polycythemia
679	neonatal diabetes mellitus
680	omenn syndrome
681	majeed syndrome
682	diabetes insipidus
683	cutis laxa
684	adiposis dolorosa
685	lymphedema
686	q fever
687	relapsing polychondritis
688	metachondromatosis
689	dubowitz syndrome
690	alpha-mannosidosis
691	craniofrontonasal dysplasia
692	poland syndrome
693	schneckenbecken dysplasia
694	ependymoma
695	hepatorenal syndrome
696	toxoplasmosis
697	lipodystrophy
698	cryoglobulinemia
699	pfeiffer syndrome
700	desquamative interstitial pneumonia

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