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Disease	Synonyms	Description
Wolff-Parkinson-White syndrome	Wolff-Parkinson-White pattern; Wolff-Parkinson-Whi.. [+] Wolff-Parkinson-White pattern; Wolff-Parkinson-White pattern (finding); Anomalous A-V excitation; anomalous atrioventricular excitation [-]	n_a
Wilson disease	Westphal-Strumpell syndrome; Wilson's disease; Wes.. [+] Wilson's disease; Westphal-Strumpell syndrome; Westphal pseudosclerosis; Cerebral pseudosclerosis; hepatolenticular degeneration [-]	n_a
Williams-Beuren syndrome	Fanconi Schlesinger syndrome	n_a
West Nile encephalitis	West Nile Fever with encephalitis; West Nile fever.. [+] West Nile Fever with encephalitis; West Nile fever encephalitis [-]	A viral infectious disease that results_in inflamm..[+] A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in West Nile virus, which is transmitted_by Culex, transmitted_by Aedes, and transmitted_by Anopheles species of mosquitoes. The infection has_symptom high fever, has_symptom headache, has_symptom neck stiffness, has_symptom stupor, has_symptom disorientation, has_symptom coma, has_symptom tremors, has_symptom convulsions, has_symptom muscle weakness, has_symptom vision loss, has_symptom numbness, and has_symptom paralysis. [-]
West Nile fever		A viral infectious disease that results_in infecti..[+] A viral infectious disease that results_in infection, has_material_basis_in West Nile virus, which is transmitted_by Culex and transmitted_by Aedes mosquitoes. The infection has_symptom fever, has_symptom sore throat, has_symptom headache, has_symptom body ache, has_symptom nausea, has_symptom maculopapular rash and has_symptom vomiting. [-]
Wernicke encephalopathy	Wernicke's encephalopathy; Wernicke's disease	A brain disease that is characterised by the prese..[+] A brain disease that is characterised by the presence of neurological symptoms of ophthalmoplegia, ataxia, and confusion caused by biochemical lesions of the central nervous system after exhaustion of B-vitamin reserves, in particular thiamine (vitamin B1). [-]
Wolffian duct adenoma	Wolffian duct adenoma; Mesonephric adenoma; Mesone.. [+] Wolffian duct adenoma; Mesonephric adenoma; Mesonephroma, benign (morphologic abnormality); benign mesonephroma; Mesonephroma, benign [-]	A reproductive organ benign neoplasm that derives_..[+] A reproductive organ benign neoplasm that derives_from glandular epithelial cells and that is located_in the region of the Wolffian duct. [-]
Wissler-Fanconi syndrome	Wissler's syndrome; Wissler-Fanconi syndrome (find.. [+] Wissler's syndrome; Wissler-Fanconi syndrome (finding); Wissler's subsepsis allergica; Wissler syndrome [-]	A syndrome that is characterized by true sepsis, a..[+] A syndrome that is characterized by true sepsis, acute rheumatic fever, rheumatoid arthritis, and adult onset Still’s disease. [-]
wheat allergy	wheat allergic reaction; allergy to wheat	n_a
Weissenbacher-Zweymuller syndrome	Piere-Robin syndrome; Pierre Robin Malformation	An osteochondrodysplasia that results_in shortened..[+] An osteochondrodysplasia that results_in shortened long bones and distinct facial abnormalities. [-]
Wolffian duct adenocarcinoma	cervical mesonephric adenocarcinoma	A cervical adenocarcinoma that has_material_basis_..[+] A cervical adenocarcinoma that has_material_basis_in remnants of mesonephric ducts and is located anywhere along the length between the ovary and vagina in sites of remnant wolffian ducts. [-]
water-clear cell adenoma	Water-clear cell adenoma (morphologic abnormality).. [+] Water-clear cell adenoma (morphologic abnormality) [-]	An adenoma that derives_from epithelial cells whic..[+] An adenoma that derives_from epithelial cells which have clear cytoplasm. [-]
Werner syndrome	Werner's syndrome; WS; adult premature ageing synd.. [+] WS; Werner's syndrome; adult premature ageing syndrome; adult progeria [-]	An autosomal recessive disease characterized by pr..[+] An autosomal recessive disease characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers. In 90% of the cases it is that has material basis in mutations in the WRN gene, on chromosome 8. [-]
well-differentiated liposarcoma	atypical lipomatous tumor	A liposarcoma that is characterized as a slow grow..[+] A liposarcoma that is characterized as a slow growing, painless tumor usually located in the retroperitoneum or the limbs and derives_from proliferating mature adipocytes. [-]
Wolffian adnexal neoplasm		n_a
Whipple disease	Whipple's disease; Whipple's disease (disorder); i.. [+] Whipple's disease (disorder); Whipple's disease; intestinal lipodystrophy [-]	n_a
Waldeyer's ring cancer	Waldeyer ring cancer; malignant neoplasm of Waldey.. [+] Waldeyer ring cancer; malignant neoplasm of Waldeyer's ring; malignant tumor of Waldeyer's ring (disorder) [-]	n_a
Wiskott-Aldrich syndrome	Wiskott syndrome	n_a
Waardenburg syndrome	Waardenburg's syndrome; Waardenburg, types I and/o.. [+] Waardenburg's syndrome; Waardenburg, types I and/or II; Waardenburg syndrome; Waardenburg Shah syndrome; van der Hoeve Halbertsona Waardenburg syndrome [-]	A syndrome characterized by varying degrees of dea..[+] A syndrome characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes. [-]
Waterhouse-Friderichsen syndrome	WFS; Meningococcal hemorrhagic adrenalitis	An adrenal gland disease that is characterized by ..[+] An adrenal gland disease that is characterized by failure of the adrenal gland due to bleeding into the gland. [-]
Wolfram syndrome	WFS; Diabetes mellitus AND insipidus with optic at.. [+] WFS; Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder); 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 gene encoding wolframin (WFS1). [-]
Western equine encephalitis	WEE	A viral infectious disease that results_in inflamm..[+] A viral infectious disease that results_in inflammation located_in brain of horses and humans, has_material_basis_in Western equine encephalomyelitis virus, which is transmitted_by Culex and transmitted_by Aedes species of mosquitoes. The infection has_symptom fever, has_symptom headache, has_symptom nausea, has_symptom vomiting, has_symptom anorexia, has_symptom malaise, has_symptom altered mental status, and has_symptom weakness. [-]
Wernicke-Korsakoff syndrome	Korsakoff Syndrome; Korsakoff's psychosis (disorde.. [+] Korsakoff Syndrome; Korsakoff's psychosis (disorder); Korsakoff's syndrome; Korsakov psychosis; Korsakov's psychosis [-]	n_a
Wegener's granulomatosis	Wegener's syndrome (disorder); Wegener granulomato.. [+] Wegener's syndrome (disorder); Wegener granulomatosis; Granulomatosis - Wegener's; Necrotizing respiratory granulomatosis [-]	An autoimmune disease that is located_in lung, loc..[+] An autoimmune disease that is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels. [-]
Werdnig-Hoffmann disease	Werdnig-Hoffman disease; hereditary motor neuropat.. [+] Werdnig-Hoffman disease; hereditary motor neuropathy proximal type I; HMN (Hereditary motor Neuropathy) Proximal type I; infantile muscular atrophy; progressive muscular atrophy of infancy; SMA1; Spinal muscular atrophy 1 [-]	A childhood spinal muscular atrophy that is a seve..[+] A childhood spinal muscular atrophy that is a severe form and is characterized by muscle weakness onset from birth to six months of age, the inability to sit unassisted. [-]
white piedra	White piedra (disorder); Tinea blanca	A superficial mycosis that is a superficial fungal..[+] A superficial mycosis that is a superficial fungal infection of the hair shaft caused by Trichosporon beigelii. Infected hairs develop soft greyish-white nodules along the shaft. [-]
Wolman disease	Wolman's or triglyceride storage type III disease; .. [+] Wolman's or triglyceride storage type III disease; Wolman's disease; Wolman xanthomatosis; Acid esterase deficiency; Acid lipase deficiency; Xanthomatosis, familial [-]	n_a
WAGR syndrome	Wilms tumor-Aniridia-Genitourinary Anomalies-Menta.. [+] Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome; 11p partial monosomy syndrome (disorder); chromosome 11p13 deletion syndrome [-]	A chromosomal deletion syndrome that is a nephrobl..[+] A chromosomal deletion syndrome that is a nephroblastoma that results_in a rare genetic syndrome in which affected children are predisposed to develop Wilms tumor, Aniridia (absence of the colored part of the eye, the iris), genitourinary anomalies, and mental retardation. The condition results from a deletion on chromosome 11 resulting in the loss of several genes. As such, it is one of the best studied examples of a condition caused by loss of neighbouring (contiguous) genes. [-]
Weaver syndrome	Weaver-Williams syndrome; WEAVER-LIKE SYNDROME	A syndrome that is characterized by prenatal and p..[+] A syndrome that is characterized by prenatal and postnatal overgrowth, accelerated osseous maturation, characteristic craniofacial appearance, and developmental delay and has_material_basis_in heterozygous mutation in the EZH2 gene on chromosome 7q36. [-]
Whitewater Arroyo hemorrhagic fever		A viral infectious disease that is a hemorrhagic f..[+] A viral infectious disease that is a hemorrhagic fever, has_material_basis_in Whitewater Arroyo virus, which is transmitted_by white-throated woodrats (Neotoma albigula). The infection has_symptom fever, has_symptom headache, has_symptom myalgia, and has_symptom hemorrhagic manifestations. [-]
wound botulism		A botulism that involves intoxication caused by bo..[+] A botulism that involves intoxication caused by botulinum neurotoxins (BoNTA, B, E and F), has_material_basis_in Clostridium botulinum A, has_material_basis_in Clostridium botulinum B, has_material_basis_in Clostridium botulinum E and has_material_basis_in Clostridium botulinum F, which are transmitted_by contact of spores with the open wounds, which then reproduce in an anaerobic environment to produce toxins. [-]
Wolf-Hirschhorn syndrome	4p deletion syndrome; chromosome 4p16.3 deletion s.. [+] 4p deletion syndrome; chromosome 4p16.3 deletion syndrome; PITT SYNDROME; Pitt-Rogers-Danks Syndrome [-]	A chromosomal deletion syndrome that is characteri..[+] A chromosomal deletion syndrome that is characterized by distinct craniofacial features, hypotonia and intellectual disability and has_material_basis_in a hemizygous deletion of chromosome 4p16.3. [-]
Weill-Marchesani syndrome	congenital mesodermal dystrophy; GEMSS syndrome; M.. [+] congenital mesodermal dystrophy; GEMSS syndrome; Marchesani-Weill Syndrome; Mesodermal Dysmorphodystrophy, Congenital; Spherophakia Brachymorphia Syndrome [-]	An autosomal genetic disease characterized by shor..[+] An autosomal genetic disease characterized by short stature, bachycephaly and other facial abnormalities, brachydactyly, joint stiffness and distinctive ocular abnormalities. [-]
Walker-Warburg syndrome	cerebroocular dysplasia-muscular dystrophy syndrom.. [+] cerebroocular dysplasia-muscular dystrophy syndrome; HARD syndrome [-]	n_a
West syndrome		n_a
withdrawal disorder		A substance-related disorder that occurs upon the ..[+] A substance-related disorder that occurs upon the abrupt discontinuation/separation or a decrease in dosage of the intake of medications, recreational drugs, and alcohol. [-]
writing disorder		A learning disability that involves impaired writt..[+] A learning disability that involves impaired written language ability such as impairments in handwriting, spelling, organization of ideas, and composition. [-]
Warburg micro syndrome	WARBM; Warburg-Sjo-Fledelius syndrome; micro syndr.. [+] Warburg-Sjo-Fledelius syndrome; WARBM; micro syndrome [-]	An autosomal recessive disease characterized by se..[+] An autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism. [-]
white shrimp allergy	Litopenaeus vannamei allergy	A crustacean allergy triggered by Litopenaeus vann..[+] A crustacean allergy triggered by Litopenaeus vannamei. [-]
Warsaw breakage syndrome	WABS	A syndrome mainly characterized by severe growth r..[+] A syndrome mainly characterized by severe growth retardation and microcephaly. It is a new form of cohesinopathy showing defects in sister chromatid cohesion and hypersensitivity to chemicals that induce replication stress, thus combining distinct cytogenetic features seen in Roberts syndrome and Fanconi anemia, respectively. It has material basis in homozygous or compound heterozygous mutation in the DDX11 gene on chromosome 12p11. [-]
WHIM syndrome	WHIMS; warts-hypogammaglobulinemia-infections-myel.. [+] WHIMS; warts-hypogammaglobulinemia-infections-myelokathexis syndrome; warts, hypogammaglobulinemia, infections, and myelokathexis [-]	An immunodeficiency disease characterized by neutr..[+] An immunodeficiency disease characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus (HPV) infection. It has material basis in heterozygous mutation in the CXCR4 gene on chromosome 2q22. [-]
Wilson-Turner syndrome	WTS; mental retardation, X-linked, syndromic 6; me.. [+] WTS; mental retardation, X-linked, syndromic 6; mental retardation, X-linked, with gynecomastia and obesity; MRXS6; X-linked intellectual disability-gynecomastia-obesity syndrome [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by intellectual disability, truncal obesity, gynecomastia, hypogonadism, dysmorphic facial features, and short stature that has_material_basis_in hemizygous mutation in the LAS1L gene on chromosome Xq12. [-]
Waldenstroem's macroglobulinemia	lymphoplasmacytic lymphoma with IgM gammopathy	A lymphoplasmacytic lymphoma characterized by the ..[+] A lymphoplasmacytic lymphoma characterized by the accumulation of monoclonal cells in the bone marrow and peripheral lymphoid tissues, and associated with the production of serum immunoglobulin M (IgM) monoclonal protein. [-]
White-Sutton syndrome	WHSUS; autosomal dominant mental retardation 37; M.. [+] WHSUS; autosomal dominant mental retardation 37; MRD37 [-]	An autosomal dominant non-syndromic intellectual d..[+] An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of POGZ on chromosome 1q21.3. [-]
wet beriberi		A beriberi that is located_in the cardiovascular s..[+] A beriberi that is located_in the cardiovascular system and has_symptom increased heart rate, swelling of lower legs, and shortness of breath. [-]
Worth's syndrome	Worth syndrome; autosomal dominant endosteal hyper.. [+] Worth syndrome; autosomal dominant endosteal hyperostosis; autosomal dominant osteosclerosis; benign form of Worth hyperostosis corticalis generalisata with torus platinus [-]	A hyperostosis that has_material_basis_in a mutati..[+] A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate. [-]
warfarin resistance		An inherited metabolic disorder that is characteri..[+] An inherited metabolic disorder that is characterized by a high tolerance for the drug warfarin. [-]
Winchester syndrome		A syndrome that is characterized by a loss of bone..[+] A syndrome that is characterized by a loss of bone tissue particularly in the hands and feet. [-]
white sponge nevus 1		A white sponge nevus that has_material_basis_in he..[+] A white sponge nevus that has_material_basis_in heterozygous mutation in the keratin-4 gene (KRT4) on chromosome 12q13. [-]
Wolcott-Rallison syndrome		A syndrome that is characterized by permanent neon..[+] A syndrome that is characterized by permanent neonatal diabetes mellitus with multiple epiphyseal dysplasia, osteoporosis, growth retardation and frequently hepatic and renal dysfunction that has_material_basis_in homozygous mutation in the eukaryotic translation initiation factor 2 alpha kinase 3 (EIF2AK3) gene on chromosome 2p11.2. [-]

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