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Disease	Synonyms	Description
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. [-]
wild-type amyloidosis	wild-type transthyretin cardiac amyloidosis; wild-.. [+] wild-type transthyretin cardiac amyloidosis; wild-type ATTR amyloidosis; Age related amyloidosis; ATTRwt amyloidosis; Old age amyloidosis; senile systemic amyloidosis [-]	An amyloidosis that is characterized by progressiv..[+] An amyloidosis that is characterized by progressive instability, misfolding and formation of amloid fibrils of the transthyretin protein. [-]
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. [-]
white sponge nevus 2		A white sponge nevus that has_material_basis_in he..[+] A white sponge nevus that has_material_basis_in heterozygous mutation in the KRT13 gene on chromosome 17q21. [-]
Wiedemann-Rautenstrauch syndrome	Neonatal progeroid syndrome; PROGEROID SYNDROME, N.. [+] Neonatal progeroid syndrome; PROGEROID SYNDROME, NEONATAL [-]	A progeroid syndrome that is characterized by intr..[+] A progeroid syndrome that is characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, and variable mental impairment and that has_material_basis_in compound heterozygous mutation in the POLR3A gene on chromosome 10q22. [-]
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. [-]
Wolfram syndrome 1	WFS1	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. [-]
Warburg micro syndrome 1	WARBM1; Micro Syndrome 1	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	WARBM2; Micro Syndrome 2	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	WARBM3; Micro Syndrome 3	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. [-]

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