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Disease	Synonyms	Description
Kuhnt-Junius degeneration	Wet senile macular retinal degeneration; Exudative.. [+] Wet senile macular retinal degeneration; Exudative senile macular degeneration of retina; Neovascular age-related macular degeneration; Senile macular degeneration, wet [-]	n_a
acute hemorrhagic leukoencephalitis	Weston-Hurst syndrome; acute haemorrhagic leucoenc.. [+] Weston-Hurst syndrome; acute haemorrhagic leucoencephalitis of Weston Hurst; acute hemorrhagic encephalomyelitis; acute necrotizing hemorrhagic leukoencephalitis; AHL [-]	A very rare form of acute disseminated encephalomy..[+] A very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema. [-]
immature cataract	Water clefts; Incipient cataract; Incipient senile.. [+] Water clefts; Incipient cataract; Incipient senile cataract [-]	A senile cataract that is characterized by variabl..[+] A senile cataract that is characterized by variable opacification of the lens of the eye with some clear lens fibers remaining. [-]
trench fever	Wolhynian fever; His-Werner disease; Quintan fever.. [+] Wolhynian fever; His-Werner disease; Quintan fever; shin bone fever; tibialgic fever; Trench fever [-]	A primary bacterial infectious disease that result..[+] A primary bacterial infectious disease that results_in systemic infection, has_material_basis_in Bartonella quintana, which is transmitted_by body lice (Pediculus humanus corporis). The infection has_symptom relapsing fever, has_symptom headache, has_symptom shin pain, and has_symptom soreness of the muscles of the legs and back. [-]
syndactyly	webbing of digits; chromosome 2q35 duplication syn.. [+] webbing of digits; chromosome 2q35 duplication syndrome; symphalangism; symphalangy [-]	A synostosis that results_in the fusion of two or ..[+] A synostosis that results_in the fusion of two or more digits. [-]
Proteus syndrome	Wiedemann's syndrome	n_a
excessive tearing	Watering eye; Epiphora; Excessive tear production; .. [+] Watering eye; Epiphora; Excessive tear production [-]	n_a
olivopontocerebellar atrophy	WADIA-SWAMI SYNDROME; Dejerine-Thomas syndrome; Th.. [+] WADIA-SWAMI SYNDROME; Dejerine-Thomas syndrome; Thomas' syndrome [-]	A neurodegenerative disease that is characterized ..[+] A neurodegenerative disease that is characterized by progressive cerebellar ataxia, leading to clumsiness in body movements, veering from midline when walking, wide-based stance, and falls without signs of paralysis or weakness and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in degeneration of neuron in the cerebellum, pons and inferior olives. [-]
inhalation anthrax	wool-sorters' disease; woolsorters' disease; pulmo.. [+] woolsorters' disease; wool-sorters' disease; pulmonary anthrax; respiratory anthrax [-]	An anthrax disease that results_in infection locat..[+] An anthrax disease that results_in infection located_in lung lymph nodes brought on by breathing in the spores of the bacteria Bacillus anthracis. The first symptoms of inhalation anthrax are like cold or flu symptoms and can include a sore throat, mild fever and muscle aches. Later symptoms include cough, chest discomfort, shortness of breath, tiredness and muscle aches. [-]
autoimmune polyendocrine syndrome type 1	Whitaker syndrom; autoimmune polyendocrinopathy-ca.. [+] Whitaker syndrom; autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy; Autoimmune Polyglandular Syndrome I [-]	An autoimmune polyendocrine syndrome that is inher..[+] An autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. [-]
tick-borne encephalitis	Western European tick-borne encephalitis; west-Sib.. [+] Western European tick-borne encephalitis; west-Siberian encephalitis; Central European encephalitis; Far Eastern TBE; Russian spring-summer encephalitis; Siberian tick-borne encephalitis; Taiga encephalitis [-]	A viral infectious disease that results_in inflamm..[+] A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in Tick-borne encephalitis virus, which is transmitted_by Ixodes ticks. The infection has_symptom drowsiness, has_symptom confusion, has_symptom sensory disturbances, and has_symptom paralysis. [-]
restless legs syndrome	Willis-Ekbom disease; Wittmaack-Ekbom syndrome; WE.. [+] Wittmaack-Ekbom syndrome; Willis-Ekbom disease; WED [-]	A central nervous system disease characterized by ..[+] A central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them. [-]
hereditary mucosal leukokeratosis	white sponge nevus of Cannon; white sponge nevus	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. [-]
seasonal affective disorder	winter depression	A mental depression that involves presentation of ..[+] A mental depression that involves presentation of depressive symptoms only during a specific season of the year. [-]
orofaciodigital syndrome VII	Whelan syndrome; OFD7	n_a
Thiel-Behnke corneal dystrophy	Waardenburg-Jonker corneal dystrophy; anterior lim.. [+] Waardenburg-Jonker corneal dystrophy; anterior limiting membrane dystrophy type II; corneal dystrophy honeycomb-shaped; corneal dystrophy of Bowman layer type II; TBCD [-]	An epithelial-stromal TGFBI dystrophy that is char..[+] An epithelial-stromal TGFBI dystrophy that is characterized by recurrent erosions and honeycomb-shaped opacification located_in the cornea, proteinaceous deposits in the anterior stroma and subepithelium, and progressive early vision loss, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation of transforming growth factor beta-induced gene located in chromosome 5q31.1, which encodes keratoepithelin. Abnormalities lead to increased protein deposition and disruption especially of Bowman's membrane of the cornea. [-]
anomalous left coronary artery from the pulmonary artery	White-Garland syndrome; ALCAPA; Bland-White-Garlan.. [+] White-Garland syndrome; ALCAPA; Bland-White-Garland syndrome [-]	A coronary artery anomaly in which the left corona..[+] A coronary artery anomaly in which the left coronary artery (LCA) branches off the pulmonary artery instead of the aortic sinus. [-]
T-cell immunodeficiency, congenital alopecia, and nail dystrophy	winged helix deficiency; alymphoid cystic thymic d.. [+] winged helix deficiency; alymphoid cystic thymic dysgenesis; severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome [-]	A severe combined immunodeficiency characterized b..[+] A severe combined immunodeficiency characterized by congenital alopecia, severe T-cell immunodeficiency, and ridging, pitting or curving of all nails that has_material_basis_in homozygous mutation in the FOXN1 gene on chromosome 17q11-q12. [-]
EEC syndrome	Walker-Clodius syndrome; ectrodactyly, ectodermal .. [+] Walker-Clodius syndrome; ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome; ectrodactyly-ectodermal dysplasia-clefting syndrome; Rudiger syndrome 1 [-]	An autosomal dominant disease characterized by ect..[+] An autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate). [-]
microphthalmia with limb anomalies	Waardenburg anophthalmia syndrome; anophthalmia-sy.. [+] Waardenburg anophthalmia syndrome; anophthalmia-syndactyly syndrome; MLA; OAS; ophthalmoacromelic syndrome [-]	A syndrome that is characterized by autosomal rece..[+] A syndrome that is characterized by autosomal recessive inheritance of bilateral or unilateral clinical anophthalmia or microphthalmia and synostosis, syndactyly, oligodactyly and/or polydactyly that has_material_basis_in homozygous mutation in the SMOC1 gene on chromosome 14q24. [-]
spastic paraplegia with deafness	Wells Jankovic Syndrome; Spastic paraparesis-deafn.. [+] Wells Jankovic Syndrome; Spastic paraparesis-deafness syndrome [-]	A hereditary spastic paraplegia that is characteri..[+] A hereditary spastic paraplegia that is characterized spastic paraplegia, tremor, cataracts, deafness, short stature, and hypogonadism presenting in the end of the first decade of life. [-]
hot water epilepsy	water immersion epilepsy; bathing epilepsy	A reflex epilepsy that is characterized by seizure..[+] A reflex epilepsy that is characterized by seizures triggered by the stimulus of bathing with hot water poured over the head. [-]
ocular albinism with sensorineural deafness	WS2-OA; autosomal recessive Waardenburg syndrome t.. [+] WS2-OA; autosomal recessive Waardenburg syndrome type 2 with ocular albinism; digenic Waardenburg syndrome/albinism; digenic Waardenburg syndrome/ocular albinism [-]	A digenic disease characterized by ocular albinism..[+] A digenic disease characterized by ocular albinism, deafness and vestibular dysfunction that has_material_basis_in mutations in the MITF gene on chromosome 3p13 and at least one other gene. The second gene mutation has been reported to be in the gene TYR on chromosome 11q14.3 and in the gene TYRP1 on chromosome 9p23. [-]
congenital muscular dystrophy-dystroglycanopathy type A11	Walker-Warburg syndrome or muscle-eye-brain diseas.. [+] Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related; congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11; MDDGA11 [-]	A congenital muscular dystrophy-dystroglycanopathy..[+] A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3. [-]
congenital muscular dystrophy-dystroglycanopathy A7	Walker-Warburg syndrome or muscle-eye-brain diseas.. [+] Walker-Warburg syndrome or muscle-eye-brain disease ISPD-related; congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A7; MDDGA7 [-]	A congenital muscular dystrophy-dystroglycanopathy..[+] A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in ISPD on 7p21.2-p21.1. [-]
congenital muscular dystrophy-dystroglycanopathy type A2	Walker-Warburg syndrome or muscle-eye-brain diseas.. [+] Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related; congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2; MDDGA2 [-]	A congenital muscular dystrophy-dystroglycanopathy..[+] A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMT2 on 14q24.3. [-]
familial woolly hair syndrome	woolly hair; wooly hair; familial wooly hair syndr.. [+] wooly hair; woolly hair; familial wooly hair syndrome; hereditary woolly hair syndrome; hereditary wooly hair syndrome [-]	A hair disease characterized by fine and tightly c..[+] A hair disease characterized by fine and tightly curled hair that grows slowly and stops growing after a few inches with hair shafts that display trichorrhexis nodosa and tapered ends. [-]

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