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Disease	Synonyms	Description	Articles	Phenotypes
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; hepatolenticular degeneration; Cerebral pseudosclerosis [-]	A metal metabolism disease that is characterized b..[+] A metal metabolism disease that is characterized by excess copper stored in various body tissues, particularly the liver, brain, and corneas of the eyes. [-]
Williams-Beuren syndrome	WBS; Fanconi Schlesinger syndrome	A syndrome that is characterized by mild to modera..[+] A syndrome that is characterized by mild to moderate intellectual disability, a broad forehead, a short nose with a broad tip, full cheeks, and a wide mouth with full lips and difficulty with visual-spatial tasks and has_material_basis_in hemizygous deletion of 1.5 to 1.8 Mb on chromosome 7q11.23. [-]	1 articles
West Nile encephalitis	West Nile fever encephalitis; West Nile Fever with.. [+] West Nile fever encephalitis; West Nile Fever with 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, Aedes, or 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 characterized by the prese..[+] A brain disease that is characterized 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 subsepsis allergica; Wissler's syndrome; .. [+] Wissler's syndrome; Wissler's subsepsis allergica; Wissler-Fanconi syndrome (finding); 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	A food allergy that develops_from exposure to and ..[+] A food allergy that develops_from exposure to and particularly consumption of wheat, and has_symptom that are both gastrointestinal and nongastrointestinal in nature, such as diarrhea, mouth and throat irritation, headache, hives, skin rashes, and anaphylaxis. [-]
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		n_a
water-clear cell adenoma	Water-clear cell adenoma; Water-clear cell adenoma.. [+] Water-clear cell adenoma; 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 [-]	A progeroid syndrome characterized by premature ag..[+] A progeroid syndrome 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 and 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); malignant tumor of Waldeyer's ring [-]	n_a
Wiskott-Aldrich syndrome	Wiskott syndrome	A syndrome that is characterized by abnormal immun..[+] A syndrome that is characterized by abnormal immune system function and a reduced ability to form blood clots resulting from a decrease in the number and size of blood cell fragments involved in clotting (microthrombocytopenia). [-]
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. [-]	3 articles
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; WS; Diabetes mellitus AND insipidus with opti.. [+] WS; WFS; Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder); DIDMOAD [-]	A syndrome that is characterized by diabetes melli..[+] A syndrome that is characterized by diabetes mellitus, optic atrophy, and deafness. [-]
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. [-]	1 articles
Wernicke-Korsakoff syndrome	Korsakoff Syndrome; Korsakoff's psychosis (disorde.. [+] Korsakoff Syndrome; Korsakoff's psychosis (disorder); Korsakoff's syndrome; Korsakov psychosis; Korsakov's psychosis; Korsakoff's psychosis [-]	A nutritional deficiency disease that is character..[+] A nutritional deficiency disease that is characterized by ophthalmoplegia, ataxia, change in mental status and acute onset of severe memory impairment without any dysfunction in intellectual abilities, and has_material_basis_in thiamine deficiency. [-]
Werdnig-Hoffmann disease	Werdnig-Hoffman disease; HMN (Hereditary motor Neu.. [+] Werdnig-Hoffman disease; HMN (Hereditary motor Neuropathy) Proximal type I; infantile muscular atrophy; hereditary motor neuropathy proximal type I; SMA1; Spinal muscular atrophy 1; progressive muscular atrophy of infancy [-]	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 and that has_material_basis_in a mutation or deletion in the telomeric copy of the SMN gene, known as SMN1, on chromosome 5q13. [-]
white piedra	White piedra (disorder); White piedra; Tinea blanc.. [+] 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 lipase deficiency; Xanthomatosis, familial; Acid esterase deficiency [-]	n_a
WAGR syndrome	Wilms tumor-Aniridia-Genitourinary Anomalies-Menta.. [+] Wilms tumor-Aniridia-Genitourinary Anomalies-Mental Retardation syndrome; chromosome 11p13 deletion syndrome; 11p partial monosomy syndrome (disorder); 11p partial monosomy 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 Mammarenavirus whitewaterense, 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. [-]
white sponge nevus	white sponge nevus of Cannon; white sponge nevus; .. [+] white sponge nevus; white sponge nevus of Cannon; hereditary mucosal leukokeratosis [-]	A skin disease characterized by a defect in the no..[+] A skin disease characterized by a defect in the normal process of keratinization of the mucosa. [-]
Wolf-Hirschhorn syndrome	PITT SYNDROME; Pitt-Rogers-Danks Syndrome; 4p dele.. [+] PITT SYNDROME; Pitt-Rogers-Danks Syndrome; 4p deletion syndrome; chromosome 4p16.3 deletion 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. [-]	5 articles	19 matches
Weill-Marchesani syndrome	congenital mesodermal dystrophy; Mesodermal Dysmor.. [+] congenital mesodermal dystrophy; Mesodermal Dysmorphodystrophy, Congenital; GEMSS syndrome; Marchesani-Weill Syndrome; Spherophakia Brachymorphia Syndrome [-]	A syndrome characterized by short stature, brachyc..[+] A syndrome characterized by short stature, brachycephaly 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 [-]	A congenital muscular dystrophy that is characteri..[+] A congenital muscular dystrophy that is characterized by hypotonia, seizures, severe intellectual and developmental disability, eye abnormalities and early death and has_material_basis_in mutations in multiple genes including POMT1, POMT2, ISPD, FKTN, FKRP, and LARGE1. [-]
West syndrome	Infantile spasms syndrome	An infancy electroclinical syndrome that is charac..[+] An infancy electroclinical syndrome that is characterized by infantile spasms, hypsarrhythmia on electroencephalogram and intellectual disability. [-]	1 articles
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	Warburg-Sjo-Fledelius syndrome; WARBM; micro syndr.. [+] WARBM; Warburg-Sjo-Fledelius syndrome; micro syndrome [-]	A syndrome characterized by severe intellectual di..[+] A syndrome 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 congenit..[+] A syndrome mainly characterized by severe congenital microcephaly, growth restriction, and sensorineural hearing loss due to cochlear hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the DDX11 gene on chromosome 12p11. [-]
WHIM syndrome	warts-hypogammaglobulinemia-infections-myelokathex.. [+] warts-hypogammaglobulinemia-infections-myelokathexis syndrome; WHIMS; warts, hypogammaglobulinemia, infections, and myelokathexis [-]	An immunodeficiency disease that is characterized ..[+] An immunodeficiency disease that is characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus infection and that 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; X-linked intellectual disability-gynecomastia-obesity syndrome; MRXS6 [-]	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. [-]
White-Sutton syndrome	WHSUS; autosomal dominant mental retardation 37; M.. [+] WHSUS; autosomal dominant mental retardation 37; MRD37 [-]	An autosomal dominant intellectual developmental d..[+] An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the POGZ gene 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. [-]
Watson syndrome		A RASopathy characterized by pulmonic stenosis, ca..[+] A RASopathy characterized by pulmonic stenosis, cafe-au-lait macules, decreased intellectual ability, and short stature that has_material_basis_in heterozygous mutation in the NF1 gene on chromosome 17q11.2. [-]
Worth syndrome	Worth syndrome; Worth's syndrome; autosomal domina.. [+] Worth's syndrome; 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. [-]
Wolfram syndrome, mitochondrial form	diabetes mellitus AND insipidus with optic atrophy.. [+] diabetes mellitus AND insipidus with optic atrophy AND deafness mitochondrial form; DIDMOAD, mitochondrial form [-]	A Wolfram syndrome that has_material_basis_in muta..[+] A Wolfram syndrome that has_material_basis_in mutation in mtDNA. [-]
warfarin resistance		An inherited metabolic disorder that is characteri..[+] An inherited metabolic disorder that is characterized by a high tolerance for the drug warfarin. [-]
warfarin sensitivity		An inherited metabolic disorder that is characteri..[+] An inherited metabolic disorder that is characterized by a low 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. [-]

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