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.

701	dysequilibrium syndrome
702	eosinophilic gastroenteritis
703	good syndrome
704	lipoma
705	myeloid leukemia
706	blepharospasm
707	rickets
708	glioma
709	acrocallosal syndrome
710	greig cephalopolysyndactyly syndrome
711	cryptosporidiosis
712	disseminated superficial actinic porokeratosis
713	strabismus
714	glioblastoma
715	lichen planus
716	brachydactyly
717	pilocytic astrocytoma
718	lymphomatoid papulosis
719	cronkhite-canada syndrome
720	pneumocystosis
721	kindler syndrome
722	keratitis
723	l-2-hydroxyglutaric aciduria
724	persistent hyperplastic primary vitreous
725	multicentric reticulohistiocytosis
726	craniodiaphyseal dysplasia
727	fish-eye disease
728	robinow syndrome
729	proximal symphalangism
730	myxoid liposarcoma
731	esophageal atresia
732	congenital syphilis
733	autosomal dominant hypophosphatemic rickets
734	arterial tortuosity syndrome
735	jarcho-levin syndrome
736	pulmonary alveolar proteinosis
737	relapsing fever
738	galactosialidosis
739	anodontia
740	vici syndrome
741	hyperostosis corticalis generalisata
742	childhood absence epilepsy
743	chronic progressive external ophthalmoplegia
744	vipoma
745	spondyloepiphyseal dysplasia tarda
746	pulmonary venoocclusive disease
747	hypothalamic hamartoma
748	macular corneal dystrophy
749	neu-laxova syndrome
750	hyperuricemia
751	protein s deficiency
752	candidiasis
753	hyperthyroidism
754	retinoschisis
755	intrahepatic cholestasis of pregnancy
756	carpenter syndrome
757	silicosis
758	pulmonary valve stenosis
759	pituitary apoplexy
760	encephalitis
761	hepatocellular adenoma
762	meckel syndrome
763	renal osteodystrophy
764	cervical intraepithelial neoplasia
765	trachoma
766	sialidosis
767	danon disease
768	pyruvate kinase deficiency
769	stargardt disease
770	conn syndrome
771	portal hypertension
772	congenital myasthenic syndrome
773	chronic myelomonocytic leukemia
774	neuroleptic malignant syndrome
775	buruli ulcer
776	primary hyperoxaluria
777	mitochondrial encephalomyopathy
778	morquio syndrome
779	giant axonal neuropathy
780	pierre robin sequence
781	coronary artery aneurysm
782	oral-facial-digital syndrome
783	angiosarcoma
784	african trypanosomiasis
785	hypoalphalipoproteinemia
786	acne rosacea
787	normal pressure hydrocephalus
788	adenomyosis
789	hemolytic anemia
790	homocystinuria due to cystathionine beta-synthase deficiency
791	focal segmental glomerulosclerosis
792	spondyloarthropathy
793	familial cold autoinflammatory syndrome
794	stiff person syndrome
795	familial hypocalciuric hypercalcemia
796	pyruvate dehydrogenase complex deficiency
797	chanarin-dorfman syndrome
798	prader willi syndrome
799	lysosomal storage disorders
800	hyper igm syndrome

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