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Disease	Synonyms	Description
Wolfram syndrome 1	WFS1; diabetes mellitus AND insipidus with optic a.. [+] WFS1; diabetes mellitus AND insipidus with optic atrophy AND deafness; DIDMOAD [-]	An autosomal recessive disease that is characteriz..[+] An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1. [-]
Wolfram syndrome 2	WFS2	An autosomal recessive neurodegenerative disorder ..[+] An autosomal recessive neurodegenerative disorder characterized by diabetes mellitus, high frequency sensorineural hearing loss, optic atrophy or neuropathy, and defective platelet aggregation resulting in peptic ulcer bleeding. It has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the CISD2 gene on chromosome 4q24. [-]
Warburg micro syndrome 1	WARBM1; Micro Syndrome 1	A Warburg micro syndrome that has_material_basis_i..[+] A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP1 gene on chromosome 2q21. [-]
Warburg micro syndrome 2	WARBM2; Micro Syndrome 2	A Warburg micro syndrome that has_material_basis_i..[+] A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP2 gene on chromosome 1q41. [-]
Warburg micro syndrome 3	WARBM3; Micro Syndrome 3	A Warburg micro syndrome that has_material_basis_i..[+] A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB18 gene on chromosome 10p12. [-]
Warburg micro syndrome 4	WARBM4; Micro Syndrome 4	A Warburg micro syndrome that has_material_basis_i..[+] A Warburg micro syndrome that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the TBC1D20 gene on chromosome 20p13. [-]
Waardenburg syndrome type 2B	WS2B; Waardenburg syndrome type IIB	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 1p21-p13.3. [-]
Waardenburg syndrome type 1	WS1; Waardenburg syndrome type I	A Waardenburg's syndrome characterized by autosoma..[+] A Waardenburg's syndrome characterized by autosomal dominant inheritance of congenital deafness, pigmentation anomalies of eyes, hair, and skin,and dystopia canthorum that has_material_basis_in heterozygous mutation in the PAX3 gene on chromosome 2q36. [-]
Waardenburg syndrome type 3	WS3; Waardenburg syndrome with upper limb anomalie.. [+] WS3; Waardenburg syndrome with upper limb anomalies; Waardenburg syndrome type III; Klein-Waardenburg syndrome [-]	A Waardenburg syndrome characterized by upper limb..[+] A Waardenburg syndrome characterized by upper limb anomalies, congenital hearing loss, dystopia canthorum and pigmentation anomalies of eyes, hair, and skin that has_material_basis_in heterozygous or homozygous mutation in the PAX3 gene on chromosome 2q36. [-]
Waardenburg syndrome type 2A	WS2A; Waardenburg syndrome type IIA	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in heterozygous mutation in the MITF gene on chromosome 3p13. [-]
Waardenburg syndrome type 2C	WS2C; Waardenburg syndrome type IIC	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in variation in the chromosome region 8p23. [-]
Waardenburg syndrome type 2D	WS2D; Waardenburg syndrome type IID	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in homozygous deletion of the SNAI2 gene on chromosome 8q11. [-]
Waardenburg syndrome type 4A	WS4A; Waardenburg syndrome with Hirschsprung disea.. [+] WS4A; Waardenburg syndrome with Hirschsprung disease type 4A; Waardenburg syndrome type IVA [-]	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous or homozygous mutation in the EDNRB gene on chromosome 13q22. [-]
Waardenburg syndrome type 4B	WS4B; Waardenburg syndrome with Hirschsprung disea.. [+] WS4B; Waardenburg syndrome with Hirschsprung disease type 4B; Waardenburg syndrome type IVB [-]	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in homozygous and heterozygous mutation in the EDN3 gene on chromosome 20q13. [-]
Waardenburg syndrome type 4C	WS4C; Waardenburg syndrome with Hirschsprung disea.. [+] WS4C; Waardenburg syndrome with Hirschsprung disease type 4C; Waardenburg syndrome type IVC [-]	A Waardenburg syndrome characterized by pigmentary..[+] A Waardenburg syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and Hirschsprung disease that has_material_basis_in heterozygous mutation in the SOX10 gene on chromosome 22q13. [-]
Waardenburg syndrome type 2E	WS2E with or without neurological involvement; WS2.. [+] WS2E with or without neurological involvement; WS2E; Waardenburg syndrome type IIE; Waardenburg syndrome type 2E with or without neurologic involvement; hypogonadotropic hypogonadism with anosmia and deafness with or without hypopigmentation [-]	A Waardenburg's syndrome characterized by pigmenta..[+] A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has_material_basis_in heterozygous mutations in the SOX10 gene on chromosome 22q13. [-]
Woodhouse-Sakati syndrome	diabetes-hypogonadism-deafness-intellectual disabi.. [+] diabetes-hypogonadism-deafness-intellectual disability syndrome; diabetes-hypogonadism-hearing loss-intellectual disability syndrome; hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome; progressive extrapyramidal disorder with primary hypogonadism, mental retardation, alopecia [-]	A syndrome characterized by hypogonadism, alopecia..[+] A syndrome characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia that has_material_basis_in homozygous or compound heterozygous mutation in the DCAF17 gene on chromosome 2q31.1. [-]
muscular atrophy	Wasting - muscle; Amyotrophia; Muscle wasting	n_a
parasitic helminthiasis infectious disease	worm infection; helminth infection; helminthiasis; .. [+] worm infection; helminth infection; helminthiasis; helminthosis [-]	A parasitic infectious disease that occurs when pa..[+] A parasitic infectious disease that occurs when part of the body is infested with parasitic worms such as cestodes, nematodes and trematodes. [-]
open-angle glaucoma	Wide-angle glaucoma; glaucoma simplex; open angle .. [+] Wide-angle glaucoma; glaucoma simplex; open angle glaucoma; pigmentary glaucoma [-]	A glaucoma characterized by optic nerve damage res..[+] A glaucoma characterized by optic nerve damage resulting in progressive loss of visual field and increased pressure in the eye due to trabecular blockage. [-]
pertussis	WC - Whooping cough; whooping cough; bordetella in.. [+] whooping cough; WC - Whooping cough; bordetella infection [-]	A commensal bacterial infectious disease that resu..[+] A commensal bacterial infectious disease that results_in inflammation located_in respiratory tract, has_material_basis_in Bordetella pertussis, or has_material_basis_in Bordetella parapertussis, which produce toxins that paralyze the cilia of the respiratory epithelial cells. The infection is characterized by a prolonged, high-pitched, deeply indrawn breath (whoop). [-]
trichuriasis	Whipworm disease; Infection by Trichuris trichura; .. [+] Whipworm disease; Infection by Trichuris trichura; Trichuriasis infection; trichuris trichiura infection [-]	A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that involves parasitic infection located_in intestine in humans, has_material_basis_in Trichuris trichiura, which is transmitted_by ingestion of food contaminated with egg-carrying soil. The infection has_symptom abdominal pain, has_symptom diarrhea, has_symptom rectal prolapse and has_symptom growth retardation. [-]
cholesterol embolism	warfarin blue toe syndrome; atheroembolism; choles.. [+] warfarin blue toe syndrome; atheroembolism; cholesterol crystal embolism; purple toe syndrome; trash foot [-]	A vascular disease that is characterized by blood ..[+] A vascular disease that is characterized by blood vessel obstruction resulting from the release of cholesterol from the inside of blood vessels along the bloodstream. [-]
nodular nonsuppurative panniculitis	Weber-Christian disease; Weber - Christian disease.. [+] Weber-Christian disease; Weber - Christian disease; nodular non-suppurative febrile panniculitis; Relapsing febrile nodular nonsuppurative panniculitis (disorder) [-]	n_a
nephroblastoma	Wilms' tumor; adult nephroblastoma; adult renal Wi.. [+] Wilms' tumor; adult nephroblastoma; adult renal Wilms' tumor; childhood renal Wilms tumor; childhood renal Wilms' cancer; renal Wilms tumor [-]	A kidney cancer that affects the kidneys and typic..[+] A kidney cancer that affects the kidneys and typically located_in children. [-]
leptospirosis	Weil's disease; Fort Bragg fever; Leptospirosis ic.. [+] Weil's disease; Fort Bragg fever; Leptospirosis icterohaemorrhagica; nanukayami fever; Rat Catcher's Yellows; spirochetal jaundice [-]	A primary bacterial infectious disease that involv..[+] A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted_by contact with water, food, or soil containing urine from the infected animals. The infection has_symptom jaundice, has_symptom chills, has_symptom fever, has_symptom muscle pain, and has_symptom hepatomegaly. [-]
gastric antral vascular ectasia	Watermelon stomach (disorder); gastric antral vasc.. [+] Watermelon stomach (disorder); gastric antral vascular ectasia (disorder) [-]	n_a
spinal cord oligodendroglioma	Well differentiated Spinal Cord Oligodendroglioma; .. [+] Well differentiated Spinal Cord Oligodendroglioma; Oligodendroglioma of spinal cord (disorder); Oligodendroglioma of spinal cord [-]	n_a
lateral medullary syndrome	Wallenberg syndrome; Posterior inferior cerebellar.. [+] Wallenberg syndrome; Posterior inferior cerebellar artery syndrome (disorder) [-]	n_a
superior mesenteric artery syndrome	Wilkie's syndrome; Superior mesenteric artery synd.. [+] Wilkie's syndrome; Superior mesenteric artery syndrome; Superior mesenteric artery syndrome (disorder) [-]	A duodenal obstruction resulting from compression ..[+] A duodenal obstruction resulting from compression of the duodenum between the aorta and the superior mesenteric artery. [-]
verrucous carcinoma	Warty carcinoma; verrucous carcinoma NOS (morpholo.. [+] Warty carcinoma; verrucous carcinoma NOS (morphologic abnormality); verrucous squamous carcinoma; verrucous squamous cell carcinoma (disorder); verrucous squamous cell carcinoma [-]	A squamous cell carcinoma that is a diffuse, papil..[+] A squamous cell carcinoma that is a diffuse, papillary, non metastasizing, well differentiated, malignant neoplasm of epidermis or oral epithelium. [-]
clear cell adenocarcinoma	Wolffian duct neoplasm; Water-clear cell carcinoma.. [+] Wolffian duct neoplasm; Water-clear cell carcinoma; Water-clear cell adenocarcinoma (morphologic abnormality); Water-Clear cell adenocarcinoma; Clear cell adenocarcinoma (morphologic abnormality); Clear cell adenocarcinoma NOS (morphologic abnormality); malignant Mesonephroma; Mesonephroid Clear cell carcinoma; mesonephroma; Mesonephroma NOS (morphologic abnormality); Mesonephroma, malignant (morphologic abnormality) [-]	An adenocarcinoma that derives_from epithelial cel..[+] An adenocarcinoma that derives_from epithelial cells which have clear cytoplasm. [-]
brain edema	wet brain; intracranial swelling	n_a
subependymal glioma	WHO grade I Ependymal tumor; mixed subependymoma-e.. [+] WHO grade I Ependymal tumor; mixed subependymoma-ependymoma; Subependymal astrocytoma; Subependymal astrocytoma NOS [-]	n_a
benign ependymoma	WHO grade II Ependymal tumor; epithelial ependymom.. [+] WHO grade II Ependymal tumor; epithelial ependymoma [-]	n_a
diffuse astrocytoma	WHO grade II astrocytoma; Diffuse astrocytoma (mor.. [+] WHO grade II astrocytoma; Diffuse astrocytoma (morphologic abnormality); Diffuse astrocytoma, low grade [-]	A low grade glioma that is characterized by diffus..[+] A low grade glioma that is characterized by diffuse infiltration of neighboring central nervous system structures. [-]
melioidosis	Whitmore's disease; acute and fulminating melioido.. [+] Whitmore's disease; acute and fulminating melioidosis; Nightcliff gardener's disease; Pseudoglanders; subacute and chronic melioidosis [-]	A primary bacterial infectious disease that result..[+] A primary bacterial infectious disease that results_in infection, has_material_basis_in Burkholderia pseudomallei, which is transmitted_by contact with the contaminated water or soil. The infection has_symptom fever, has_symptom respiratory distress, has_symptom chest pain, and has_symptom stomach pain. [-]
hereditary Wilms' tumor	WT1; Hereditary Wilms tumor; hereditary Wilms' tum.. [+] WT1; Hereditary Wilms tumor; hereditary Wilms' tumor [-]	A nephroblastoma that results_in either bilateral ..[+] A nephroblastoma that results_in either bilateral disease or a family history of Wilms' tumour. [-]
benign intermediate mesothelioma	Well-differentiated Papillary tumor of Mesothelium.. [+] Well-differentiated Papillary tumor of Mesothelium [-]	n_a
congestive heart failure	Weak heart; Cardiac Failure Congestive; CHF; Conge.. [+] Weak heart; Cardiac Failure Congestive; CHF; Congestive heart disease [-]	A heart disease that is characterized by any struc..[+] A heart disease that is characterized by any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. [-]
tooth and nail syndrome	Witkop's syndrome; Hypoplastic enamel-onycholysis-.. [+] Witkop's syndrome; Hypoplastic enamel-onycholysis-hypohidrosis syndrome; Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder); Tooth and Nail syndrome [-]	A syndrome that affects the teeth, nails, hair, an..[+] A syndrome that affects the teeth, nails, hair, and/or skin. It is characterized by absence (hypodontia) and/or malformation of certain primary (deciduous) and secondary (permanent) teeth occurring in association with improper development of the nails, particularly the toenails. [-]
mixed oligodendroglioma-astrocytoma	WHO grade II mixed glioma	n_a
epithelial malignant thymoma	Well differentiated thymic carcinoma; Squamoid Thy.. [+] Well differentiated thymic carcinoma; Squamoid Thymoma; Thymoma, epithelial [-]	n_a
intermediate coronary syndrome	Worsening angina; (Angina: [crescendo] or [unstabl.. [+] Worsening angina; (Angina: [crescendo] or [unstable] or [at rest]) or (preinfarction syndrome) or (impending infarction); Angina at rest; Anginal chest pain at rest; Impending infarction (disorder); Preinfarction angina; Preinfarction angina (disorder); Unstable angina [-]	n_a
autoimmune thrombocytopenic purpura	werlhof's disease; Autoimmune thrombocytopenic pur.. [+] werlhof's disease; Autoimmune thrombocytopenic purpura; Ideopath thrombocytopenic pur; Idiopathic purpura; idiopathic thrombocytopenic purpura; Immune thrombocytopenic purpura (disorder); primary thrombocytopenic purpura; Immune thrombocytopenic purpura [-]	A primary thrombocytopenia that involves relativel..[+] A primary thrombocytopenia that involves relatively few platelets in blood as a result of autoantibodies. [-]
variola minor	whitepox; Alastrim; cottonpox; milkpox; Variola mi.. [+] whitepox; Alastrim; cottonpox; milkpox; Variola minor [-]	A smallpox that results_in milder infection, locat..[+] A smallpox that results_in milder infection, located_in skin, has_material_basis_in Variola virus. The infection results_in_formation_of lesions. [-]
frontotemporal dementia	Wilhemsen-Lynch disease; frontotemporal lobar dege.. [+] Wilhemsen-Lynch disease; frontotemporal lobar degeneration; multiple system tauopathy with presenile dementia; pallidopontonigral degeneration [-]	A basal ganglia disease characterized by progressi..[+] A basal ganglia disease characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. [-]
multiple endocrine neoplasia type 2B	Wagenmann-Froboese syndrome; MEN type IIB; MEN2B; .. [+] Wagenmann-Froboese syndrome; MEN type IIB; MEN2B; mucosal neuroma syndrome; multiple endocrine neoplasia type 2b; Multiple endocrine neoplasia, type 3 [-]	A multiple endocrine neoplasia characterized by me..[+] A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. [-]
multiple endocrine neoplasia type 1	Wermer syndrome; Wermer's syndrome; MEN type I; mu.. [+] Wermer's syndrome; Wermer syndrome; MEN type I; multiple endocrine neoplasia type 1 [-]	An autosomal dominant disease that has_material_ba..[+] An autosomal dominant disease that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas. [-]
conjunctival pterygium	Web eye	A pterygium that is characterized by conjunctival ..[+] A pterygium that is characterized by conjunctival degeneration, a fleshy outpouching of conjunctival growth and has_symptom fleshy bumps on the surface of the eye, foreign body sensation, decreased vision, and astigmatism. Conjunctival pterygiums are more common in people prone to ocular surface injury, such as those living in sunny, hot, and dry climates. Conjunctival pterygiums progress from pinguecula. [-]

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