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Disease	Synonyms	Description
Waldeyer's ring cancer	malignant neoplasm of Waldeyer's ring; malignant t.. [+] malignant neoplasm of Waldeyer's ring; malignant tumor of Waldeyer's ring (disorder); Waldeyer ring cancer; [-]	n_a
Walker-Warburg syndrome	cerebroocular dysplasia-muscular dystrophy syndrom.. [+] cerebroocular dysplasia-muscular dystrophy syndrome; HARD syndrome; [-]	n_a
Warburg micro syndrome	micro syndrome; WARBM; Warburg-Sjo-Fledelius syndr.. [+] micro syndrome; WARBM; Warburg-Sjo-Fledelius 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. [-]
Warburg micro syndrome 1	Micro Syndrome 1; WARBM1;	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	Micro Syndrome 2; WARBM2;	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	Micro Syndrome 3; WARBM3;	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	Micro Syndrome 4; WARBM4;	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. [-]
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. [-]
Waterhouse-Friderichsen syndrome	Meningococcal hemorrhagic adrenalitis; WFS;	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. [-]
Weaver syndrome	WEAVER-LIKE SYNDROME; Weaver-Williams 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. [-]
Wegener's granulomatosis	Granulomatosis - Wegener's; Necrotizing respirator.. [+] Granulomatosis - Wegener's; Necrotizing respiratory granulomatosis; Wegener granulomatosis; Wegener's syndrome (disorder); [-]	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. [-]
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. [-]
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. [-]
Werdnig-Hoffmann disease	hereditary motor neuropathy proximal type I; HMN (.. [+] hereditary motor neuropathy proximal type I; HMN (Hereditary motor Neuropathy) Proximal type I; infantile muscular atrophy; progressive muscular atrophy of infancy; Werdnig-Hoffman disease; 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. [-]
Werner syndrome	adult premature ageing syndrome; adult progeria; W.. [+] adult premature ageing syndrome; adult progeria; Werner's syndrome; WS; [-]	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. [-]
Wernicke encephalopathy	Wernicke's disease; Wernicke's encephalopathy;	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). [-]
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
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, 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. [-]
West syndrome		n_a
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. [-]
Whipple disease	intestinal lipodystrophy; Whipple's disease; Whipp.. [+] intestinal lipodystrophy; Whipple's disease; Whipple's disease (disorder); [-]	n_a
White-Sutton syndrome	autosomal dominant mental retardation 37; MRD37; W.. [+] autosomal dominant mental retardation 37; MRD37; WHSUS; [-]	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. [-]
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. [-]
Williams-Beuren syndrome	Fanconi Schlesinger syndrome;	n_a
Wilson disease	Cerebral pseudosclerosis; hepatolenticular degener.. [+] Cerebral pseudosclerosis; hepatolenticular degeneration; Westphal pseudosclerosis; Westphal-Strumpell syndrome; Wilson's disease; [-]	n_a
Wilson-Turner syndrome	mental retardation, X-linked, syndromic 6; mental .. [+] mental retardation, X-linked, syndromic 6; mental retardation, X-linked, with gynecomastia and obesity; MRXS6; WTS; 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. [-]
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. [-]
Wiskott-Aldrich syndrome	Wiskott syndrome;	n_a
Wissler-Fanconi syndrome	Wissler syndrome; Wissler's subsepsis allergica; W.. [+] Wissler syndrome; Wissler's subsepsis allergica; Wissler-Fanconi syndrome (finding); Wissler's 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. [-]
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. [-]
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. [-]
Wolff-Parkinson-White syndrome	Anomalous A-V excitation; anomalous atrioventricul.. [+] Anomalous A-V excitation; anomalous atrioventricular excitation; Wolff-Parkinson-White pattern (finding); Wolff-Parkinson-White pattern; [-]	n_a
Wolffian adnexal neoplasm		n_a
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. [-]
Wolffian duct adenoma	Mesonephric adenoma; Mesonephroma, benign (morphol.. [+] Mesonephric adenoma; Mesonephroma, benign (morphologic abnormality); Wolffian duct adenoma; 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. [-]
Wolfram syndrome	Diabetes mellitus AND insipidus with optic atrophy.. [+] Diabetes mellitus AND insipidus with optic atrophy AND deafness (disorder); DIDMOAD; WFS; [-]	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). [-]
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. [-]
Wolman disease	Acid esterase deficiency; Acid lipase deficiency; .. [+] Acid esterase deficiency; Acid lipase deficiency; Wolman xanthomatosis; Wolman's disease; Wolman's or triglyceride storage type III disease; Xanthomatosis, familial; [-]	n_a
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. [-]
Worth's syndrome	autosomal dominant endosteal hyperostosis; autosom.. [+] autosomal dominant endosteal hyperostosis; autosomal dominant osteosclerosis; benign form of Worth hyperostosis corticalis generalisata with torus platinus; Worth syndrome; [-]	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. [-]
X-linked Aarskog syndrome	Aarskog-Scott syndrome; faciogenital dysplasia; Gr.. [+] Aarskog-Scott syndrome; faciogenital dysplasia; Greig's syndrome; [-]	A syndromic X-linked intellectual disability affec..[+] A syndromic X-linked intellectual disability affects a person's height, muscles, skeleton, genitals, and appearance of the face. [-]
X-linked Alport syndrome	ATS; nephropathy and deafness, X-linked;	An Alport syndrome that has_material -basis_in mut..[+] An Alport syndrome that has_material -basis_in mutation in the gene encoding the alpha-5 chain of basement membrane collagen type IV (COL4A5). [-]
X-linked Emery-Dreifuss muscular dystrophy 6	EDMD6; Emery-Dreifuss muscular dystrophy 6, X-link.. [+] EDMD6; Emery-Dreifuss muscular dystrophy 6, X-linked; myopathy, X-linked, with postural muscle atrophy; XMPMA; [-]	An Emery-Dreifuss muscular dystrophy that has_mate..[+] An Emery-Dreifuss muscular dystrophy that has_material_basis_in an X-linked recessive mutation of the FHL1 gene on chromosome Xq26.3. [-]
X-linked adrenal hypoplasia congenita	congenital adrenal hypoplasia;	An adrenal cortical hypofunction that is character..[+] An adrenal cortical hypofunction that is characterized by a reduction in adrenal gland function resulting from incomplete development of the adrenal cortex and has_material_basis_in the nuclear receptor NR0B1 (DAX1) gene. [-]
X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2	AIH3; amelogenesis imperfecta type IE X-linked 2 .. [+] AIH3; amelogenesis imperfecta type IE X-linked 2 ; amelogenesis imperfecta 3 hypoplastic type; X-linked enamel hypoplasia; [-]	An amelogenesis imperfecta associated with mutatio..[+] An amelogenesis imperfecta associated with mutation in a gene in the Xq22-q28 region. [-]
X-linked cardiac valvular dysplasia	CVD1; Dystrophie valvulaire associee a FLNA; EDS 5.. [+] CVD1; Dystrophie valvulaire associee a FLNA; EDS 5; Ehlers-Danlos syndrome, type 5; Filamin A-related X-linked myxomatous valvular dysplasia; FLNA-related valvular dystrophy; FLNA-related X-linked myxomatous valvular dysplasia; XMVD; [-]	A heart valve disease characterized by multivalvul..[+] A heart valve disease characterized by multivalvular dysplasia and regurgitation with more severe phenotypes in hemizygous males compared to heterozygous females that has_material_basis_in mutation in the FLNA gene on chromosome Xq28. [-]
X-linked chondrodysplasia punctata	chondrodystrophia calcificans congenita;	n_a
X-linked cleft palate with or without ankyloglossia	X-linked cleft palate and ankyloglossia;	A cleft palate that has_material_basis in mutation..[+] A cleft palate that has_material_basis in mutation in the TBX22 gene on chromosome Xq21. [-]

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