eRAM

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.

About 15942 Results.

ID	Disease
1901	glossopharyngeal neuralgia
1902	embryonal carcinoma
1903	nephrogenic syndrome of inappropriate antidiuresis
1904	lymphangiosarcoma
1905	weyers acrofacial dysostosis
1906	mesangial proliferative glomerulonephritis
1907	ovarian fibroma
1908	tricuspid atresia
1909	ivemark syndrome
1910	phaeohyphomycosis
1911	atypical hemolytic uremic syndrome
1912	scott syndrome
1913	mercury poisoning
1914	empty sella syndrome
1915	keratomalacia
1916	partington syndrome
1917	lethal midline granuloma
1918	aromatic l-amino acid decarboxylase deficiency
1919	laryngoonychocutaneous syndrome
1920	familial progressive hyperpigmentation
1921	posterior urethral valve
1922	ablepharon macrostomia syndrome
1923	collecting duct carcinoma
1924	nasu-hakola disease
1925	amish lethal microcephaly
1926	cerebro-costo-mandibular syndrome
1927	congenital dyserythropoietic anemia type iii
1928	kikuchi disease
1929	familial gestational hyperthyroidism
1930	drug-induced lupus erythematosus
1931	recurrent acute pancreatitis
1932	spondylocarpotarsal synostosis
1933	megalencephaly-capillary malformation-polymicrogyria syndrome
1934	molybdenum cofactor deficiency
1935	benign familial neonatal seizures
1936	syndromic diarrhea
1937	griscelli syndrome
1938	galactose epimerase deficiency
1939	papillorenal syndrome
1940	sarcosinemia
1941	craniofacial-deafness-hand syndrome
1942	orthostatic hypotension
1943	hypothalamic disease
1944	cicatricial alopecia
1945	serkal syndrome
1946	epidemic typhus
1947	olivopontocerebellar atrophy
1948	hereditary sensory and autonomic neuropathy type 1
1949	x-linked adrenal hypoplasia congenita
1950	renal oncocytoma
1951	carrion's disease
1952	dissecting cellulitis of the scalp
1953	ohtahara syndrome
1954	median arcuate ligament syndrome
1955	auriculo-condylar syndrome
1956	acute erythroid leukemia
1957	monosomy 22q13
1958	stargardt disease 1
1959	locked in syndrome
1960	meige disease
1961	hypolipoproteinemia
1962	hyperthermia
1963	fukuyama type congenital muscular dystrophy
1964	renpenning syndrome
1965	hypertrichotic osteochondrodysplasia
1966	plasma cell leukemia
1967	scapuloperoneal spinal muscular atrophy
1968	hereditary neutrophilia
1969	stormorken syndrome
1970	arts syndrome
1971	childhood apraxia of speech
1972	acquired porencephaly
1973	2q37 deletion syndrome
1974	whitaker syndrome
1975	hereditary sensory and autonomic neuropathy type iv
1976	multiple familial trichoepithelioma
1977	tolosa hunt syndrome
1978	congenital bilateral perisylvian syndrome
1979	michels syndrome
1980	atelosteogenesis
1981	familial paroxysmal kinesigenic dyskinesia
1982	sed congenita
1983	branchio oculo facial syndrome
1984	gaba-transaminase deficiency
1985	antley bixler syndrome
1986	familial atrial fibrillation
1987	toxic encephalopathy
1988	acromesomelic dysplasia, maroteaux type
1989	ceroid lipofuscinosis, neuronal, 3
1990	ectodermal dysplasia 1, hypohidrotic, x-linked
1991	acyl-coa dehydrogenase, medium chain, deficiency of
1992	acyl-coa dehydrogenase, short-chain, deficiency of
1993	acrocapitofemoral dysplasia
1994	aneurysmal bone cysts
1995	congenital nephrotic syndrome, finnish type
1996	carnitine deficiency, systemic primary
1997	anaplastic oligoastrocytoma
1998	diaphanospondylodysostosis
1999	differentiated thyroid carcinoma
2000	congenital hydrocephalus

Rare Disease
Rett syndrome ;
Scleroderma ;
Coats disease ;
Cyclic neutropenia ;
Cystinuria