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Disease	Synonyms	Description	Articles
diffuse glioma, H3 G34 mutant		A histone mutated tumor that has_material_basis_in..[+] A histone mutated tumor that has_material_basis_in mutations in codon 34 of the H3 histone family 3A protein. [-]
diffuse glomerulonephritis		n_a
diffuse idiopathic skeletal hyperostosis	Ankylosing vertebral hyperostosis; DISH; Forestier.. [+] Ankylosing vertebral hyperostosis; DISH; Forestier disease; Disseminated idiopathic skeletal hyperostosis; [-]	A calcinosis that is the calcification or a bony h..[+] A calcinosis that is the calcification or a bony hardening of ligaments in areas where they attach to your spine. [-]
diffuse infiltrative lymphocytosis syndrome		A syndrome that occurs in human immunodeficiency v..[+] A syndrome that occurs in human immunodeficiency virus (HIV) positive patients, which is accompanied by decreased kidney function. The spectrum of kidney involvement includes acute or chronic kidney disease, primarily tubular proteinuria and dense lymphocytic tubulointerstitial infiltrates predominantly composed of CD8 T cells. [-]
diffuse interstitial keratitis		n_a
diffuse large B-cell lymphoma	DLBCL;	A large B-cell lymphoma that is consisting of medi..[+] A large B-cell lymphoma that is consisting of medium-sized to large B cells with a diffuse growth pattern. [-]
diffuse large B-cell lymphoma activated B-cell type	DLBCL ABC type;	A diffuse large B-cell lymphoma that is characteri..[+] A diffuse large B-cell lymphoma that is characterized by the expression of CD44, PKCbeta1, Cyclin D2, BCL-2, and IRF4/MUM1 genes. [-]
diffuse large B-cell lymphoma germinal center B-cell type		A diffuse large B-cell lymphoma that is characteri..[+] A diffuse large B-cell lymphoma that is characterized by the expression of CD10, BCL-6, A-myb, and LMO2 genes, BCL-2 translocation, and c-REL amplification. [-]
diffuse leptomeningeal glioneuronal tumor	Diffuse leptomeningeal glioneuronal tumour;	A central nervous system benign neoplasm that is c..[+] A central nervous system benign neoplasm that is characterized by the presence of clear glial neoplastic cells reminiscent of oligodendroglioma. [-]
diffuse lipomatosis		n_a
diffuse low-grade glioma, MAPK pathway–altered		A low grade glioma that is characterized by a gene..[+] A low grade glioma that is characterized by a gene alteration that results in a MAPK pathway abnormality, with morphological features of astrocytoma or oligodendroglioma. [-]
diffuse meningeal melanocytosis	Diffuse melanocytosis (morphologic abnormality); D.. [+] Diffuse melanocytosis (morphologic abnormality); Diffuse Melanosis; Diffuse melanocytosis; Meningeal melanocytosis; [-]	A central nervous system melanocytic neoplasm that..[+] A central nervous system melanocytic neoplasm that is characterized as diffuse or multifocal proliferation of uniform nevoid polygonal cells in the leptomeninges. [-]
diffuse midline glioma, H3 K27M-mutant	diffuse intrinsic pontine glioma;	A histone mutated tumor that is characterized by t..[+] A histone mutated tumor that is characterized by the presence of histone H3 K27M mutation located throughout the midline structures of the central nervous system. [-]
diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype	diffuse paediatric-type high-grade glioma, H3-wild.. [+] diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype; [-]	A high grade glioma that is characterized by the a..[+] A high grade glioma that is characterized by the absence of histone H3, IDH1, and IDH2 mutations. [-]
diffuse peritoneal leiomyomatosis	leiomyomatosis peritonealis disseminata (disorder).. [+] leiomyomatosis peritonealis disseminata (disorder); leiomyomatosis peritonealis disseminata; [-]	A peritoneal benign neoplasm that is located throu..[+] A peritoneal benign neoplasm that is located throughout the peritoneum and derives_from smooth muscle. [-]
diffuse pulmonary fibrosis		n_a
diffuse scleroderma	systemic sclerosis, diffuse (disorder); diffuse sy.. [+] systemic sclerosis, diffuse (disorder); diffuse systemic sclerosis; systemic sclerosis, diffuse; [-]	n_a
diffuse secondary choroid atrophy		n_a
dihydropyrimidinase deficiency	dihydropyrimidinuria; DPH deficiency; DPYSD; DPYS .. [+] dihydropyrimidinuria; DPH deficiency; DPYSD; DPYS deficiency; [-]	A pyrimidine metabolic disorder characterized by a..[+] A pyrimidine metabolic disorder characterized by a defect in the degredation of uracil and thymine resulting in elevated levels of 5,6-dihydrouracil and 5,6-dihydrothymine in urine that has_material_basis_in homozygous or compound heterozygous mutation in the DPYS gene on chromosome 8q22.3. [-]
dihydropyrimidine dehydrogenase deficiency	Dihydropyrimidine dehydrogenase deficiency (disord.. [+] Dihydropyrimidine dehydrogenase deficiency (disorder); familial pyrimidinaemia; Dihydropyrimidine dehydrogenase deficiency; thymine-uracilurea ; Dihydrouracil Dehydrogenase deficiency; [-]	A purine-pyrimidine metabolic disorder that is an ..[+] A purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. [-]
dilated cardiomyopathy	Idiopathic dilation cardiomyopathy; primary dilate.. [+] Idiopathic dilation cardiomyopathy; primary dilated cardiomyopathy; Congestive cardiomyopathy; Familial dilated cardiomyopathy; [-]	An intrinsic cardiomyopathy that is characterized ..[+] An intrinsic cardiomyopathy that is characterized by an an enlarged heart and damage to the myocardium causing the heart to pump blood inefficiently. [-]	3 articles
dilated cardiomyopathy 1A	CDCD1; CMD1A; dilated cardiomyopathy with conducti.. [+] CDCD1; CMD1A; dilated cardiomyopathy with conduction defect 1; familial dilated cardiomyopathy with conduction defect due to LMNA mutation; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the LMNA gene on chromosome 1q21. [-]
dilated cardiomyopathy 1AA	CMD1AA; dilated cardiomyopathy 1AA with or without.. [+] CMD1AA; dilated cardiomyopathy 1AA with or without left ventricular noncompaction; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the ACTN2 gene on chromosome 1q43. [-]
dilated cardiomyopathy 1B	CMD1B;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 9q13. [-]
dilated cardiomyopathy 1BB	CMD1BB;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation the DSG2 gene on chromosome 18q12.1. [-]
dilated cardiomyopathy 1C	CMDC1; dilated cardiomyopathy 1C with or without l.. [+] CMDC1; dilated cardiomyopathy 1C with or without left ventricular noncompaction; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the LDB3 gene on chromosome 10q23.2. [-]
dilated cardiomyopathy 1CC	CMD1CC;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the NEXN gene on chromosome 1p31.1. [-]
dilated cardiomyopathy 1D	CMD1D;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the TNNT2 gene on chromosome 1q32. [-]
dilated cardiomyopathy 1DD	CMD1DD;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the RBM20 gene on chromosome 10q25. [-]
dilated cardiomyopathy 1E	CDCD2; CMD1E; dilated cardiomyopathy with conducti.. [+] CDCD2; CMD1E; dilated cardiomyopathy with conduction defect 2; dilated cardiomyopathy with conduction disorder and arrhythmia; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the SCN5A gene on chromosome 3p22.2. [-]
dilated cardiomyopathy 1EE	CMD1EE;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the MYH6 gene on chromosome 14q11.2. [-]
dilated cardiomyopathy 1FF	CMD1FF;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the TNNI3 gene on chromosome 19q13.42. [-]
dilated cardiomyopathy 1G	CMD1G;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the TTN gene on chromosome 2q31. [-]
dilated cardiomyopathy 1GG	CMD1GG;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the SDHA gene on chromosome 5p15.33. [-]
dilated cardiomyopathy 1H	dilated cardiomyopathy with conduction defect; CMD.. [+] dilated cardiomyopathy with conduction defect; CMD1H; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 2q14-q22. [-]
dilated cardiomyopathy 1HH	CMD1HH;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the BAG3 gene on chromosome 10q26.11. [-]
dilated cardiomyopathy 1I	CMD1I;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the DES gene on chromosome 2q35. [-]
dilated cardiomyopathy 1II	CMD1II;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the CRYAB gene on chromosome 11q23. [-]
dilated cardiomyopathy 1J	autosomal dominant dilated cardiomyopathy with sen.. [+] autosomal dominant dilated cardiomyopathy with sensorineural hearing loss; CMD1J; neurosensory deafness with dilated cardiomyopathy; neurosensory hearing loss with dilated cardiomyopathy; sensorineural deafness with dilated cardiomyopathy; sensorineural hearing loss with dilated cardiomyopathy; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.2. [-]
dilated cardiomyopathy 1JJ	CMD1JJ;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the LAMA4 gene on chromosome 6q21. [-]
dilated cardiomyopathy 1K	CMD1K;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 6q12-q16. [-]
dilated cardiomyopathy 1KK	CMD1KK;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the MYPN gene on chromosome 10q21. [-]
dilated cardiomyopathy 1L	CMD1L;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutations in the SGCD gene on chromosome 5q33.2-q33.3. [-]
dilated cardiomyopathy 1LL		A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in heterozygous mutation in the PRDM16 gene on chromosome 1p36. [-]
dilated cardiomyopathy 1M	CMD1M;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the CSRP3 gene on chromosome 11p15. [-]
dilated cardiomyopathy 1MM		A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in heterozygous mutation in the MYBPC3 gene on chromosome 11p11. [-]
dilated cardiomyopathy 1NN	CMD1NN;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the RAF1 gene on chromosome 3p25. [-]
dilated cardiomyopathy 1O	CMD1O; dilated cardiomyopathy with ventricular tac.. [+] CMD1O; dilated cardiomyopathy with ventricular tachycardia; [-]	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the ABCC9 gene on chromosome 12p12.1. [-]
dilated cardiomyopathy 1P	CMD1P;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in mutation in the PLN gene on chromosome 6q22. [-]
dilated cardiomyopathy 1Q	CMD1Q;	A dilated cardiomyopathy that has_material_basis_i..[+] A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 7q22.3-q31.1. [-]

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