- Encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis - SeeAicardi-Goutieres syndrome
- Encephalopathy, familial, with Collins bodies - See Familial encephalopathy with neuroserpin inclusion bodies
- Encephalopathy, hepatic - See Hepatic encephalopathy
- Encephalopathy, petechiae, and ethylmalonic aciduria - See Ethylmalonic encephalopathy
- Encephalopathy, recurrent, of childhood - See Neuhauser Eichner Opitz syndrome
- Encephalotrigeminal angiomatosis - See Sturge-Weber syndrome
- Enchondroma
- Enchondromatosis - See Ollier disease
- Enchondromatosis dwarfism deafness
- Enchondromatosis with Multiple Cavernous Hemangiomas - See Maffucci syndrome
- Endemic Kaposi sarcoma
- Endemic pemphigus foliaceus - See Pemphigus and fogo selvagem
- Endemic syphilis - See Bejel
- Endemic treponematoses - See Yaws
- Endemic treponematosis caused by Treponema carateum - See Pinta
- Endemic typhus - See Typhus
- Endocardial fibroelastosis
- Endocarditis, infective - See Infective endocarditis
- Endocrine adenomatosis multiple - See Multiple endocrine neoplasia type 1
- Endodermal-sinus tumor - See Testicular yolk sac tumor
- Endoepithelial corneal dystrophy - See Fuchs endothelial corneal dystrophy - not a rare disease
- Endogenous hypertriglyceridaemia - See Familial lipoprotein lipase deficiency
- Endolymphatic sac tumor
- Endometrial Adenosquamous Cancer - See Adenosquamous carcinoma of the endometrium
- Endometrial Adenosquamous Carcinoma - See Adenosquamous carcinoma of the endometrium
- Endometrial stromal sarcoma
- Endomyocardial fibroelastosis
- Endomyocardial fibrosis
- Endosteal hyperostosis autosomal recessive - See Hyperostosis corticalis generalisata
- Endosteal hyperostosis, autosomal dominant - See Worth type autosomal dominant osteosclerosis
- Endosteal hyperostosis, Worth type - See Worth type autosomal dominant osteosclerosis
- ENFL1 - See Autosomal dominant nocturnal frontal lobe epilepsy
- Engelhard Yatziv syndrome
- Engelmann disease - See Camurati-Engelmann disease
- Engraftment syndrome
- Enhanced S-cone syndrome - See Goldmann-Favre syndrome
- Enlarged heart and poor heart function - See Keshan disease
- Enlarged tongue - See Macroglossia
- Enlarged vestibular aqueduct syndrome
- Enolase 3 deficiency - See Glycogen storage disease type 13
- Enolase-beta deficiency - See Glycogen storage disease type 13
- Enteric fever - See Typhoid fever
- Enteritis - See Crohn's disease - not a rare disease
- Enterocolitis, necrotizing - See Necrotizing enterocolitis
- Enterocyte cobalamin malabsorption - See Imerslund-Grasbeck syndrome
- Enteropathica
- Enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy - See Immunodysregulation, polyendocrinopathy and enteropathy X-linked
- Enteropathy-associated T-cell lymphoma
- Enterovesical fistula
- Enterovirus antenatal infection
- Enthesitis related arthritis, juvenile - See Enthesitis-related juvenile idiopathic arthritis
- Enthesitis-related arthritis - See Enthesitis-related juvenile idiopathic arthritis
- Enthesitis-related JIA - See Enthesitis-related juvenile idiopathic arthritis
- Enthesitis-related juvenile idiopathic arthritis
- Envenomization by bothrops lanceolatus
- Envenomization by the Martinique lancehead viper - See Envenomization by bothrops lanceolatus
- EOC - See Ovarian epithelial cancer
- EOCA - See Harding ataxia
- EOCA-HA - See Ataxia with oculomotor apraxia type 1
- EOF - See Polyostotic osteolytic dysplasia, hereditary expansile
- EOFAD - See Early-onset, autosomal dominant Alzheimer disease
- Eosinophil peroxidase deficiency
- Eosinophil peroxidase deficiency, partial - See Eosinophil peroxidase deficiency
- Eosinophilia-myalgia syndrome
- Eosinophilic angiocentric fibrosis - See EAF
- Eosinophilic cellulitis - See Wells syndrome
- Eosinophilic cryptitis
- Eosinophilic cystitis
- Eosinophilic enteritis - See Eosinophilic enteropathy
- Eosinophilic enteropathy
- Eosinophilic esophagitis - See Eosinophilic enteropathy
- Eosinophilic fasciitis
- Eosinophilic folliculitis - See Eosinophilic pustular folliculitis
- Eosinophilic folliculitis, pustular - See Eosinophilic pustular folliculitis
- Eosinophilic gastritis - See Eosinophilic enteropathy
- Eosinophilic gastroenteritis - See Eosinophilic enteropathy
- Eosinophilic gastroenteropathy - See Eosinophilic enteropathy
- Eosinophilic glassy cell hepatoma - See Fibrolamellar carcinoma
- Eosinophilic granuloma of soft tissue - See Kimura disease
- Eosinophilic granulomatosis with polyangiitis
- Eosinophilic hepatocellular carcinoma with lamellar fibrosis - See Fibrolamellar carcinoma
- Eosinophilic hyperplastic lymphogranuloma - See Kimura disease
- Eosinophilic idiopathic chronic pneumopathy - See Chronic eosinophilic pneumonia (CEP)
- Eosinophilic lymphofollicular granuloma - See Kimura disease
- Eosinophilic lymphofolliculosis - See Kimura disease
- Eosinophilic lymphogranuloma - See Kimura disease
- Eosinophilic mastitis
- Eosinophilic pustular folliculitis
- EOTD - See DYT-TOR1A
- EPEMA syndrome - See Ethylmalonic encephalopathy
- Ependymoblastoma - See Embryonal tumor with multilayered rosettes
- Ependymoma
- Ependymoma, familial - See Ependymoma
- EPF - See Eosinophilic pustular folliculitis
- Epidemic typhus - See Typhus
- Epidermal nevus - not a rare disease
- Epidermal nevus vitamin D resistant rickets
- Epidermodysplasia verruciformis
- Epidermoid brain cyst
- Epidermoid brain tumor - See Epidermoid brain cyst
- Epidermoid carcinoma - See Squamous cell carcinoma - not a rare disease
- Epidermolysa bullosa simplex and limb girdle muscular dystrophy - See Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysis bullosa
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa atrophicans - See Junctional epidermolysis bullosa
- Epidermolysis bullosa dystrophica - See Dystrophic epidermolysis bullosa
- Epidermolysis bullosa dystrophica, autosomal dominant - See Dominant dystrophic epidermolysis bullosa
- Epidermolysis bullosa dystrophica, Cockayne-Touraine type (formerly) - See Dominant dystrophic epidermolysis bullosa
- Epidermolysis bullosa dystrophica, dominant neonatal form - See Transient bullous dermolysis of the newborn
- Epidermolysis bullosa dystrophica, Pasini type (formerly) - See Dominant dystrophic epidermolysis bullosa
- Epidermolysis bullosa herpetiformis, Dowling-Meara type - See Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa intraepidermic - See Epidermolysis bullosa simplex
- Epidermolysis bullosa junctionalis with pyloric atresia - See Epidermolysis bullosa
- Epidermolysis bullosa junctionalis, non-Herlitz type - See Epidermolysis bullosa
- Epidermolysis bullosa letalis - See Epidermolysis bullosa
- Epidermolysis bullosa macular type - See Bullous dystrophy hereditary macular type
- Epidermolysis bullosa of hands and feet - See Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa simplex
- Epidermolysis bullosa simplex - limb girdle muscular dystrophy - See Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysis bullosa simplex due to plakophilin deficiency - See Ectodermal dysplasia skin fragility syndrome
- Epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders - See Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
- Epidermolysis bullosa simplex of palms and soles - See Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, generalized non-Dowling-Meara - See Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, herpetiformis - See Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa simplex, Koebner type - See Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa simplex, Ogna type
- Epidermolysis bullosa simplex, Weber-Cockayne type - See Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa with pyloric atresia - See Epidermolysis bullosa
- Epidermolysis bullosa, dermolytic - See Dystrophic epidermolysis bullosa
- Epidermolysis bullosa, junctional - See Junctional epidermolysis bullosa
- Epidermolysis bullosa, junctional, Herlitz type - See Epidermolysis bullosa
- Epidermolysis bullosa, junctional, Herlitz-Pearson type - See Epidermolysis bullosa
- Epidermolysis bullosa, junctional, non-Herlitz type - See Epidermolysis bullosa
- Epidermolysis bullosa, lethal acantholytic
- epidermolytic hyperkeratosis - See Epidermolytic ichthyosis
- Epidermolytic ichthyosis
- Epidermolytic palmoplantar keratoderma
- Epidermolytic palmoplantar keratoderma of Voerner - See Epidermolytic palmoplantar keratoderma
- Epidermolytic palmoplantar keratoderma of Vörner - See Epidermolytic palmoplantar keratoderma
- Epidermolytic palmoplantar keratoderma Vorner type - See Palmoplantar keratoderma, epidermolytic
- Epidermolytic palmoplantar keratoderma woolly hair and dilated cardiomyopathy - See Cardiomyopathy dilated with woolly hair and keratoderma
- Epilepsy - microcephaly - skeletal dysplasia - See Battaglia-Neri syndrome
- Epilepsy and mental retardation limited to females - See PCDH19-related female-limited epilepsy
- Epilepsy and yellow teeth - See Kohlschutter Tonz syndrome
- Epilepsy dementia amelogenesis imperfecta - See Kohlschutter Tonz syndrome
- Epilepsy juvenile absence
- Epilepsy mental deterioration Finnish type
- Epilepsy occipital calcifications
- Epilepsy progressive myoclonic 2 - See Lafora disease
- Epilepsy progressive myoclonic type 3
- Epilepsy syndrome, infantile-onset symptomatic - See GM3 synthase deficiency
- Epilepsy telangiectasia
- Epilepsy with bilateral occipital calcifications - See Epilepsy occipital calcifications
- Epilepsy with myoclonic-astatic seizures - See Epilepsy with myoclonic-atonic seizures
- Epilepsy with myoclonic-atonic seizures
- Epilepsy with myoclono-astatic crisis - See Epilepsy with myoclonic-atonic seizures
- Epilepsy, ataxia, sensorineural deafness and tubulopathy - See SeSAME syndrome
- Epilepsy, benign neonatal, with Myokymia - See Myokymia with neonatal epilepsy
- Epilepsy, benign neonatal-infantile - See Benign familial neonatal-infantile seizures
- Epilepsy, benign occipital
- Epilepsy, familial temporal lobe - See Temporal epilepsy, familial
- Epilepsy, female restricted, with mental retardation - See PCDH19-related female-limited epilepsy
- Epilepsy, nocturnal frontal lobe, 1 - See Autosomal dominant nocturnal frontal lobe epilepsy
- Epilepsy, partial, familial
- Epilepsy, progressive myoclonic type 1 - See Unverricht-Lundborg disease
- Epilepsy, progressive myoclonus 1 - See Unverricht-Lundborg disease
- Epilepsy-ataxia-sensorineural deafness-tubulopathy syndrome - See SeSAME syndrome
- Epileptic encephalopathy Lennox-Gastaut type - See Lennox-Gastaut syndrome
- Epileptic encephalopathy with continuous spike-and-wave during slow sleep - See Continuous spike-wave during slow sleep syndrome
- Epileptic encephalopathy, childhood-onset - See CHD2 myoclonic encephalopathy
- Epileptic encephalopathy, early infantile, 10 - See Early Infantile Epileptic Encephalopathy
- Epileptic encephalopathy, early infantile, 12 - See Early Infantile Epileptic Encephalopathy 12
- Epileptic Encephalopathy, early infantile, 13 - See SCN8A encephalopathy
- EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 22; EIEE22 - See SLC35A2-CDG
- Epileptic encephalopathy, early infantile, 9 - See PCDH19-related female-limited epilepsy
- Epimerase deficiency galactosemia - See Galactose epimerase deficiency
- Epimetaphyseal dysplasia cataract
- Epiphyseal dysplasia dysmorphism camptodactyly
- Epiphyseal dysplasia hearing loss dysmorphism
- Epiphyseal dysplasia multiple 1 - See Multiple epiphyseal dysplasia 1
- Epiphyseal dysplasia multiple 2 - See Multiple epiphyseal dysplasia 2
- Epiphyseal dysplasia multiple 3 - See Multiple epiphyseal dysplasia 3
- Epiphyseal dysplasia multiple 4 - See Multiple epiphyseal dysplasia 4
- Epiphyseal dysplasia multiple 5 - See Multiple epiphyseal dysplasia 5
- Epiphyseal dysplasia multiple with early-onset diabetes mellitus
- Epiphyseal dysplasia, microcephaly and nystagmus - See Lowry Wood syndrome
- Epiphyseal dysplasia, multiple - See Multiple epiphyseal dysplasia
- Epiphyseal stippling with osteoclastic hyperplasia - See Pacman dysplasia
- Episkopi blindness - See Norrie disease
- Episodic angioedema with eosinophilia
- Episodic ataxia
- Episodic Ataxia syndrome - See Episodic ataxia
- Episodic ataxia type 2 - See Episodic ataxia with nystagmus
- Episodic ataxia with nystagmus
- Episodic encephalopathy due to thiamine pyrophosphokinase deficiency - See Childhood encephalopathy due to thiamine pyrophosphokinase deficiency
- Episodic kinesigenic dyskinesia 1 - See Paroxysmal kinesigenic choreoathetosis
- Epithelial basement membrane corneal dystrophy
- Epithelial ependymoma - See Ependymoma
- Epithelial myoepithelial carcinoma - See Epithelial-myoepithelial carcinoma
- Epithelial ovarian cancer - See Ovarian epithelial cancer
- Epithelial tumor of thymus - See Thymic epithelial tumor
- Epithelial-myoepithelial carcinoma
- Epithelioid sarcoma
- Epithelioma adenoides cysticum - See Multiple familial trichoepithelioma
- Epitheliopathy, acute posterior multifocal placoid pigment - See Acute posterior multifocal placoid pigment epitheliopathy
- EPM 3 - See Epilepsy progressive myoclonic type 3
- EPM1 - See Unverricht-Lundborg disease
- EPM2 - See Lafora disease
- EPM6 - See GOSR2-related progressive myoclonus ataxia
- EPP - See Erythropoietic protoporphyria
- EPPK - See Epidermolytic palmoplantar keratoderma
- EPPK - See Palmoplantar keratoderma, epidermolytic
- EPS - See Elastosis perforans serpiginosa
- Epstein Barr virus infection, familial fatal - See X-linked lymphoproliferative syndrome
- Epstein syndrome - See MYH9 related thrombocytopenia
- EPXD - See Eosinophil peroxidase deficiency
- Equine morbillivirus (formerly) - See Nipah virus encephalitis
- ERA - See Enthesitis-related juvenile idiopathic arthritis
- Erb-Goldflam syndrome - See Myasthenia gravis congenital
- Erdheim Chester disease - See Erdheim-Chester disease
- Erdheim cystic medial necrosis of aorta - See Cystic medial necrosis of aorta
- Erdheim disease - See Cystic medial necrosis of aorta
- Erdheim-Chester disease
- Ergotism - See St Anthony's fire
- Erlacher-Blount syndrome - See Blount disease
- Ermine phenotype
- ERMS - See Rhabdomyosarcoma embryonal
- Erosive adenomatosis of the nipple - See Florid papillomatosis of the nipple
- Erosive pustular dermatosis of the scalp
- Erosive vitreoretinopathy - See Wagner syndrome
- ERS - See Amelogenesis imperfecta nephrocalcinosis
- ERS - See Amelogenesis imperfecta hypoplastic type, IG
- ERVR - See Wagner syndrome
- Erysipelas
- Erythema elevatum diutinum
- Erythema migrans - See Geographic tongue - not a rare disease
- Erythema multiforme
- Erythema multiforme bullosum - See Erythema multiforme
- Erythema nodosum of unknown etiology - See Erythema nodosum, idiopathic
- Erythema nodosum, familial - See Familial erythema nodosum
- Erythema nodosum, idiopathic
- Erythema polymorphe, erythema multiforme type - See Erythema multiforme
- Erythroblastic anemia - See Beta-thalassemia
- Erythroblastopenia, transient - See Transient erythroblastopenia of childhood
- Erythrocytosis autosomal dominant benign - See Primary familial and congenital polycythemia
- Erythroderma desquamativa of Leiner
- Erythroderma Desquamativum of Infancy - See Erythroderma desquamativa of Leiner
- Erythroderma lethal congenital
- Erythrodermic ichthyosis - See Nonbullous congenital ichthyosiform erythroderma
- Erythrogenesis imperfecta - See Diamond-Blackfan anemia
- Erythrohepatic protoporphyria - See Erythropoietic protoporphyria
- Erythroid 5-aminolevulinate synthase deficiency - See X-linked sideroblastic anemia
- Erythrokeratoderma "en cocardes" - See Degos 'en cocarde' erythrokeratoderma
- Erythrokeratodermia - ataxia - See Spinocerebellar ataxia 34
- Erythrokeratodermia figurata, congenital familial, in plaques - See Keratoderma palmoplantaris transgrediens
- Erythrokeratodermia variabilis - See Erythrokeratodermia variabilis et progressiva
- Erythrokeratodermia variabilis et progressiva
- Erythrokeratodermia variabilis with erythema gyratum repens - See Keratoderma palmoplantaris transgrediens
- Erythrokeratodermia variabilis, Mendes da Costa type - See Erythrokeratodermia variabilis et progressiva
- Erythrokeratodermia with ataxia - See Spinocerebellar ataxia 34
- Erythrokeratodermia, progressive symmetric - See Erythrokeratodermia variabilis et progressiva
- Erythrokeratolysis hiemalis ichthyosis - See Keratolytic winter erythema
- Erythroleukemia - See Acute erythroid leukemia
- Erythromelalgia
- Erythroplakia
- Erythropoietic protoporphyria
- Erythropoietic uroporphyria associated with myeloid malignancy
- ES - See Benign eccrine spiradenoma
- Escher Hirt syndrome
- Escobar syndrome - See Multiple pterygium syndrome Escobar type
- Escobar syndrome, type B
- Escobar variant multiple pterygium syndrome - See Multiple pterygium syndrome Escobar type
- Escobar variant with pursed mouth, creased tongue, ophthalmologic features, and scoliosis - See Escobar syndrome, type B
- Esophageal achalasia - See Idiopathic achalasia
- Esophageal atresia
- Esophageal atresia coloboma talipes
- Esophageal cancer
- Esophageal cancer, childhood
- Esophageal varices
- Esophagitis-peptic ulcer - See Barrett esophagus - not a rare disease
- Esophagogastric and vulvar leiomyomatosis - See Leiomyoma of vulva and esophagus
- Esophagus cancer - See Esophageal cancer
- Esotropia
- ESS - See Endometrial stromal sarcoma
- ESS1 (formerly) - See Multiple self healing squamous epithelioma
- Essential benign fructosuria - See Fructosuria - not a rare disease
- Essential thrombocythemia
- Essential thrombocytosis - See Essential thrombocythemia
- Essential tremor - not a rare disease
- Essential tremors, nystagmus and duodenal ulceration - See Tremors, nystagmus and duodenal ulcers
- EST - See Mediastinal endodermal sinus tumors
- Esthesioneuroblastoma - See Olfactory neuroblastoma
- ETANTR - See Embryonal tumor with multilayered rosettes
- Ethylmalonic encephalopathy
- Ethylmalonic-adipicaciduria - See Glutaric acidemia type II
- ETL1 - See Autosomal dominant partial epilepsy with auditory features
- ETM1 - See Tremor hereditary essential, 1
- ETM2 - See Tremor hereditary essential, 2
- ETMR - See Embryonal tumor with multilayered rosettes
- Eulenburg disease - See Paramyotonia congenita
- Eunuchoidism familial hypogonadotropic
- Eunuchoidism with spermatogenesis, normal FSH and low or normal interstitial cell-stimulating hormone (ICSH) - SeeFertile eunuch syndrome
- EUOS - See Urethral obstruction sequence
- Evan syndrome - See Evans syndrome
- Evans syndrome
- EVMPS - See Multiple pterygium syndrome Escobar type
- Ewing family of tumors - See Ewing's family of tumors
- Ewing sarcoma
- Ewing tumor - See Ewing sarcoma
- Ewing’s tumor of bone (type) - See Ewing's family of tumors
- Ewing's family of tumors
- Ewing's sarcoma - See Ewing sarcoma
- Ewing's tumor - See Ewing sarcoma
- Exaggerated physiologic speckled mottling of skin - See Bier spots
- Exaggerated startle reaction - See Hereditary hyperekplexia
- Exaggerated startle reflex - See Jumping Frenchmen of Maine
- Excess of mature unencapsulated fatty tissue in the pelvis - See Pelvic lipomatosis
- Exencephaly
- Exercise induced hyperinsulinemic hypoglycemia - See Exercise-induced hyperinsulinemic hypoglycemia
- Exercise-induced anaphylaxis
- Exercise-induced hyperinsulinemic hypoglycemia
- Exertional headache
- Exfoliative dermatitis
- Exogenous lipoid pneumonia
- Exogenous ochronosis
- Exomphalos macroglossia gigantism syndrome - See Beckwith-Wiedemann syndrome
- Exophthalmic goiter - See Graves' disease
- Exostoses anetodermia brachydactyly type E
- Exostoses, multiple, type 1
- Exostoses, multiple, type 2
- Exostoses, multiple, type 3
- Expanded spectrum hemifacial microsomia - See Goldenhar disease
- Expanded spectrum of hemifacial microsomia - See Goldenhar disease
- Expansile osteolysis, familial - See Polyostotic osteolytic dysplasia, hereditary expansile
- Experimental silicosis - See Silicosis
- Exstrophy of the bladder
- Exstrophy-epispadias complex
- Extra digits - See Polydactyly
- Extra nipple - See Supernumerary nipple - not a rare disease
- Extracardiac Rhabdomyoma
- Extracranial arteriovenous malformation
- Extracranial AVM - See Extracranial arteriovenous malformation
- Extragonadal germ cell tumor
- Extrahepatic bile duct cancer - See Bile duct cancer
- Extramammary Paget disease
- Extramedullary myeloid tumor - See Myeloid sarcoma
- Extramembranous glomerulonephritis - See Membranous nephropathy
- Extranodal nasal NK/T cell lymphoma
- Extraosseous Ewing’s (tumor growing outside of the bone) (type) - See Ewing's family of tumors
- Extraovarian Brenner tumor of the vagina - See Brenner tumor of the vagina
- Extrasystoles short stature hyperpigmentation microcephaly
- Extreme hirsutism with gingival fibromatosis - See Gingival fibromatosis with hypertrichosis
- Extrinsic allergic pneumonia hypersensitivity Pneumonitis - See Hypersensitivity pneumonitis
- Exudative retinopathy with bone marrow failure - See Revesz syndrome
- Exudative vitreoretinopathy, familial - See Familial exudative vitreoretinopathy
- Exulceratio simplex Dieulafoy - See Dieulafoy lesion
- Eye cancer, retinoblastoma - See Retinoblastoma
- Eye defects arachnodactyly cardiopathy - See Al Gazali syndrome
- Eyebrows duplication of, with stretchable skin and syndactyly
- Eyelashes, long with intellectual disability - See Trichomegaly with intellectual disability, dwarfism and pigmentary degeneration of retina
- EZH2 Related Overgrowth - See Weaver syndrome
sábado, 26 de enero de 2019
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
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