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Disease	Synonyms	Description	Articles
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 syndrome characterized by pigmentary..[+] A Waardenburg 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 syndrome characterized by autosomal ..[+] A Waardenburg 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 type III; Waardenburg sy.. [+] Waardenburg syndrome type III; WS3; Waardenburg syndrome with upper limb anomalies; 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 syndrome characterized by pigmentary..[+] A Waardenburg 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 syndrome characterized by pigmentary..[+] A Waardenburg 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 4A	Waardenburg syndrome type IVA; WS4A; Waardenburg s.. [+] WS4A; Waardenburg syndrome type IVA; Waardenburg syndrome with Hirschsprung disease type 4A [-]	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 or homozygous mutation in the EDNRB gene on chromosome 13q22. [-]
Waardenburg syndrome type 4B	Waardenburg syndrome with Hirschsprung disease typ.. [+] Waardenburg syndrome with Hirschsprung disease type 4B; Waardenburg syndrome type IVB; WS4B [-]	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 homozygous and heterozygous mutation in the EDN3 gene on chromosome 20q13. [-]
Waardenburg syndrome type 4C	Waardenburg syndrome with Hirschsprung disease typ.. [+] Waardenburg syndrome with Hirschsprung disease type 4C; Waardenburg syndrome type IVC; WS4C [-]	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 syndrome characterized by pigmentary..[+] A Waardenburg 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. [-]
Weyers acrofacial dysostosis	WAD; Weyers acrodental dysostosis; acrofacial dyso.. [+] Weyers acrodental dysostosis; WAD; acrofacial dysostosis, Weyers type; Curry-Hall syndrome [-]	An acrofacial dysostosis characterized by dental a..[+] An acrofacial dysostosis characterized by dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature that has_material_basis_in heterozygous mutation in the genes EVC2 or EVC on chromosome 4p16.2. [-]
Waisman syndrome	early-onset parkinsonism-intellectual disability s.. [+] early-onset parkinsonism-intellectual disability syndrome; Laxova-Opitz syndrome [-]	A syndrome characterized by delayed psychomotor de..[+] A syndrome characterized by delayed psychomotor development, impaired intellectual development, and early-onset Parkinson disease that has_material_basis_in hemizygous or homozygous mutation in the RAB39B gene on chromosome Xq28. [-]
wrinkly skin syndrome	WSS	A syndrome characterized by sagging or wrinkly ski..[+] A syndrome characterized by sagging or wrinkly skin, reduced skin elasticity, delayed closure of the fontanel, typically mild developmental delay, and variable other skeletal, neurological and facial features that has_material_basis_in homozygous or compound heterozygous mutation in the ATP6V0A2 gene on chromosome 12q24.31. [-]
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	1 articles
parasitic helminthiasis infectious disease	worm infection; helminthiasis; helminth infection; .. [+] worm infection; helminthiasis; helminth infection; 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; cholesterol crystal em.. [+] warfarin blue toe syndrome; cholesterol crystal embolism; trash foot; purple toe syndrome; atheroembolism [-]	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. [-]

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