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Disease	Synonyms	Description	Articles
distal 10q deletion syndrome	chromosome 10q26 deletion syndrome; monosomy 10qte.. [+] chromosome 10q26 deletion syndrome; monosomy 10qter; telomeric deletion 10q; terminal chromosome 10q26 deletion syndrome; distal monosomy 10q; [-]	n_a
distal arthrogryposis	Arthrogryposis Multiplex Congenita; Freeman-Sheldo.. [+] Arthrogryposis Multiplex Congenita; Freeman-Sheldon syndrome; Sheldon-Hall syndrome; Freeman-Sheldon syndrome variant; [-]	A muscle tissue disease characterized by congenita..[+] A muscle tissue disease characterized by congenital joint contractures of hand and feet. [-]	3 articles
distal arthrogryposis type 1	DA1; digitotalar dysmorphism;	A distal arthrogryposis characterized by autosomal..[+] A distal arthrogryposis characterized by autosomal domiant inheritance of contractures of the distal regions of the hands and feet with no facial involvement or other anomalies. [-]
distal arthrogryposis type 10	DA10; short Achilles tendon; short tendo calcaneus.. [+] DA10; short Achilles tendon; short tendo calcaneus; plantar flexion contracture; [-]	A distal arthrogryposis that has_material_basis_in..[+] A distal arthrogryposis that has_material_basis_in heterozygous mutation in the chromosome region 2q31.3-q32.1. [-]
distal arthrogryposis type 1A	DA1A;	A distal arthrogryposis type 1 that has_material_b..[+] A distal arthrogryposis type 1 that has_material_basis_in heterozygous mutation in the TPM2 gene on chromosome 9p13.3. [-]
distal arthrogryposis type 1B	DA1B;	A distal arthrogryposis type 1 that has_material_b..[+] A distal arthrogryposis type 1 that has_material_basis_in heterozygous mutation in the MYBPC1 gene on chromosome 12q23.2. [-]
distal arthrogryposis type 1C	DA1C;	A distal arthrogryposis type 1 characterized by co..[+] A distal arthrogryposis type 1 characterized by congenital contractures, scoliosis, and short stature that has_material_basis_in heterozygous or homozygous mutation in the MYLPF gene on chromosome 16p11.2. [-]
distal arthrogryposis type 2A	DA2A; distal arthrogryposis type 2A (Freeman-Sheld.. [+] DA2A; distal arthrogryposis type 2A (Freeman-Sheldon); [-]	A Freeman-Sheldon syndrome that has_material_basis..[+] A Freeman-Sheldon syndrome that has_material_basis_in heterozygous mutation in the MYH3 gene on chromosome 17p13.1. [-]
distal arthrogryposis type 2B	DA2B; Freeman-Sheldon syndrome variant; Sheldon-Ha.. [+] DA2B; Freeman-Sheldon syndrome variant; Sheldon-Hall syndrome; [-]	A distal arthrogryposis characterized by contractu..[+] A distal arthrogryposis characterized by contractures of the distal joints of the limbs, triangular face, downslanting palpebral fissures, small mouth, and high arched palate. [-]
distal arthrogryposis type 2B1	DA2B1;	A distal arthrogryposis type 2B that has_material_..[+] A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the TNNI2 gene on chromosome 11p15.5. [-]
distal arthrogryposis type 2B2	DA2B2;	A distal arthrogryposis type 2B that has_material_..[+] A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the TNNT3 gene on chromosome 11p15.5. [-]
distal arthrogryposis type 2B3	DA2B3; distal arthrogryposis type 2B3 (Sheldon-Hal.. [+] DA2B3; distal arthrogryposis type 2B3 (Sheldon-Hall); [-]	A distal arthrogryposis type 2B that has_material_..[+] A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the MYH3 gene on chromosome 17p13.1. [-]
distal arthrogryposis type 3	camptodactyly-cleft palate-clubfoot syndrome; DA3;.. [+] camptodactyly-cleft palate-clubfoot syndrome; DA3; distal arthrogryposis multiplex congenita type IIA; Gordon syndrome; [-]	A distal arthrogryposis characterized by distal ar..[+] A distal arthrogryposis characterized by distal arthrogryposis with short stature and cleft palate that has_material_basis_in heterozygous mutation in the PIEZO2 gene on chromosome 18p11.22-p11.21. [-]
distal arthrogryposis type 4	DA4; distal arthrogryposis type IID; DAIID; arthro.. [+] DA4; distal arthrogryposis type IID; DAIID; arthrogryposis-severe scoliosis syndrome; [-]	A distal arthrogryposis characterized by distal ar..[+] A distal arthrogryposis characterized by distal arthrogryposis with severe scoliosis. [-]
distal arthrogryposis type 5	DA5; DAIIB; distal arthrogryposis with ophthalmopl.. [+] DA5; DAIIB; distal arthrogryposis with ophthalmoplegia; oculomelic amyoplasia; arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome; distal arthrogryposis type IIB; [-]	A distal arthrogryposis characterized by distal ar..[+] A distal arthrogryposis characterized by distal arthrogryposis with ocular abnormalities that has_material_basis_in heterozygous gain of function mutation in the PIEZO2 gene on chromosome 18p11.22-p11.21. [-]
distal arthrogryposis type 5D	DA5D; distal arthrogryposis type 5 without ophthal.. [+] DA5D; distal arthrogryposis type 5 without ophthalmoparesis; distal arthrogryposis type 5 without ophthalmoplegia; [-]	A distal arthrogryposis characterized by severe ca..[+] A distal arthrogryposis characterized by severe camptodactyly of the hands, mild camptodactyly of the toes, extension contractures of the knee, and distinctive facial features that has_material_basis_in homozygous or compound heterozygous mutation in the ECEL1 gene on chromosome 2q37.1. [-]
distal arthrogryposis type 6	DA6; familial hand abnormality and sensori-neural .. [+] DA6; familial hand abnormality and sensori-neural deafness; arthrogryposis-like hand anomaly-sensorineural deafness syndrome; arthrogryposis and sensorineural deafness; [-]	A distal arthrogryposis characterized by distal ar..[+] A distal arthrogryposis characterized by distal arthrogryposis with sensorineural deafness. [-]
distal arthrogryposis type 7	DA7; Dutch-Kentucky syndrome; Hecht syndrome; Hech.. [+] DA7; Dutch-Kentucky syndrome; Hecht syndrome; Hecht-Beals syndrome; mouth, inability to completely open, and short finger-flexor tendons; trismus-pseudocamptodactyly syndrome; [-]	A distal arthrogryposis characterized by inability..[+] A distal arthrogryposis characterized by inability to open the mouth fully and pseudocamptodactyly that has_material_basis_in heterozygous mutation in the MYH8 gene on chromosome 17p13.1. [-]
distal biliary tract carcinoma	carcinoma of the Distal biliary tract;	n_a
distal myopathy	distal myopathy; Miyoshi muscular dystrophy; dista.. [+] distal myopathy; Miyoshi muscular dystrophy; distal muscular dystrophy; [-]	A muscular dystrophy that is characterized by pred..[+] A muscular dystrophy that is characterized by predominant weakness and atrophy beginning in the feet and/or hands. [-]
distal myopathy 1	Distal myopathy type 1; Gowers disease; Laing dist.. [+] Distal myopathy type 1; Gowers disease; Laing distal myopathy; Laing early-onset distal myopathy; MPD1; [-]	A distal myopathy that is characterized by autosom..[+] A distal myopathy that is characterized by autosomal dominant inheritance that has_material_basis_in mutation in the MYH7 gene on chromosome 14q11.2. [-]
distal myopathy 3	distal myopathy 3; distal myopathy type 3; MPD3; d.. [+] distal myopathy 3; distal myopathy type 3; MPD3; distal muscular dystrophy 3; [-]	A distal myopathy that is characterized by adult o..[+] A distal myopathy that is characterized by adult onset of slowly progressive distal muscular weakness and atrophy affecting the upper and lower limbs, leading to difficulties using the hands and walking difficulties and that has significant linkage to 2 distinct regions on chromosomes 8p22-q11 and 12q13-q22 and that has_material_basis_in heterozygous mutation in the HNRNPA1 gene on chromosome 12q13. [-]
distal myopathy 4	distal ABD-filaminopathy; distal myopathy 4; dista.. [+] distal ABD-filaminopathy; distal myopathy 4; distal myopathy with posterior leg and anterior hand involvement; MPD4; distal muscular dystrophy 4; [-]	A distal myopathy that has_material_basis_in heter..[+] A distal myopathy that has_material_basis_in heterozygous mutation in FLNC on 7q32. [-]
distal myopathy Tateyama type	distal muscular dystrophy Tateyama type;	A distal myopathy that has_material_basis_in heter..[+] A distal myopathy that has_material_basis_in heterozygous mutation in the caveolin-3 gene (CAV3) on chromosome 3p25. [-]
distal myopathy with anterior tibial onset	DMAT; distal muscular dystrophy with anterior tibi.. [+] DMAT; distal muscular dystrophy with anterior tibial onset; [-]	A distal myopathy that is characterized by onset a..[+] A distal myopathy that is characterized by onset at 14-28 years of age starting first in the anterior tibial muscles and involving both upper and lower proximal muscles that has_material_basis_in homozygous mutation in the gene encoding dysferlin (DYSF) on chromosome 2p13. [-]
distal myopathy with rimmed vacuoles		A distal myopathy that is characterized by adult o..[+] A distal myopathy that is characterized by adult onset of muscle weakness affecting the distal upper and lower limbs, which may result in walking difficulties, as well as proximal weakness of the shoulder girdle muscles and that has_material_basis_in by heterozygous mutation in the SQSTM1 gene on chromosome 5q35. [-]
diversion colitis		A colitis caused_by diversion of the fecal stream ..[+] A colitis caused_by diversion of the fecal stream due to complication of ileostomy or colostomy. [-]
diverticulitis		An intestinal disease characterized by the formati..[+] An intestinal disease characterized by the formation and inflammation of diverticula within the bowel wall. [-]
diverticulitis of colon	colonic diverticular disease;	A colonic disease characterized by the formation a..[+] A colonic disease characterized by the formation and inflammation of diverticula within the colon wall. [-]
dominant optic atrophy plus syndrome	optic atrophy with or without deafness, ophthalmop.. [+] optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy; DOA+; [-]	A syndrome characterized by visual loss and sensor..[+] A syndrome characterized by visual loss and sensorineural hearing loss with onset in childhood and associated with other symptoms including; progressive external ophthalmoplegia, muscle cramps, hyperreflexia, and ataxia that has_material_basis_in heterozygous mutation in the OPA1 gene on chromosome 3q29. [-]
dominant pericentral pigmentary retinopathy		A retinitis pigmentosa that is characterized pigme..[+] A retinitis pigmentosa that is characterized pigmentary retinal degeneration with onset in the teens leading to blindness in the sixth ans seventh decades of life. [-]
dopamine beta-hydroxylase deficiency	norepinephrine deficiency; noradrenaline deficienc.. [+] norepinephrine deficiency; noradrenaline deficiency; congenital dopamine beta-hydroxylase deficiency; [-]	An inherited metabolic disorder characterized by d..[+] An inherited metabolic disorder characterized by decreased beta-hydroxylation of dopamine in nerves resulting in impaired autonomic noradrenergic neurotransmission and clinical features including severely decreased norepinephrine levels, orthostatic hypotension, ptosis, nasal stuffiness, and delayed eye opening that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the dopamine beta-hydroxylase gene (DBH) on chromosome 9q34. [-]
dopamine transporter deficiency syndrome	DTDS;	A movement disease characterized by parkinsonism-d..[+] A movement disease characterized by parkinsonism-dystonia including tremor, progressive bradykinesia, and dystonic posturing that has_material_basis_in mutation in the SLC6A3 gene on chromosome 5p15.33. [-]
double outlet right ventricle	Double outlet right ventricle (disorder); Double o.. [+] Double outlet right ventricle (disorder); Double outlet right ventricle NOS (disorder); Double outlet right ventricle with subpulmonary ventricular septal defect; Taussig-Bing syndrome or defect; Dextrotransposition of aorta (disorder); Double outlet right ventricle, unspecified (disorder); Double outlet right ventricle; Dextrotransposition of aorta; [-]	n_a
double pterygium		A pterygium that is characterized by a fleshy outp..[+] A pterygium that is characterized by a fleshy outpouching of conjunctival growth that appears to have multiple heads or areas of bulk or origin and has_symptom multiple fleshy bumps on the surface of the eye, foreign body sensation, decreased vision, and astigmatism. Double pterygiums are more common in people prone to ocular surface injury, such as those living in sunny, hot, and dry climates. Double pterygiums progress from pinguecula. [-]
dracunculiasis	Dracontiasis; Infection by Dracunculus medinensis;.. [+] Dracontiasis; Infection by Dracunculus medinensis; Infection by Dracunculus medinensis (disorder); [-]	A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that involves parasitic infection by the larvae of the nematode Dracunculus medinensis, which are transmitted to humans by drinking water containing copepods infected with the larvae. The female, which contains larvae, burrows into the deeper connective tissues or adjacent to long bones or joints of the extremities. The worm emerges as a whitish filament in the center of a painful ulcer, accompanied by inflammation and frequently by secondary bacterial infection. [-]
dropped head syndrome	floppy head syndrome;	A spinal disease that is characterized by severe k..[+] A spinal disease that is characterized by severe kyphotic deformity of the cervicothoracic spine and by severe weakness of the cervical paraspinal muscles that results in the passively correctable chin-on-chest deformity. This syndrome is defined by weakness of neck extensor muscles against gravity with or without weakness of neck flexor muscles. [-]
drug allergy		A hypersensitivity reaction type I disease trigger..[+] A hypersensitivity reaction type I disease triggered by a drug. [-]
drug dependence		A substance dependence that involves the continued..[+] A substance dependence that involves the continued use of drugs despite problems related to use of the substance. [-]
drug psychosis	Drug-induced psychotic disorder; Drug-induced psyc.. [+] Drug-induced psychotic disorder; Drug-induced psychosis; [-]	n_a
drug-induced hepatitis	Drug-induced chronic hepatitis (disorder); Drug-in.. [+] Drug-induced chronic hepatitis (disorder); Drug-induced chronic hepatitis; [-]	n_a
drug-induced lupus erythematosus	DILE; DIL;	A lupus erythematosus caused by chronic use of cer..[+] A lupus erythematosus caused by chronic use of certain drugs. [-]
drug-induced mental disorder		n_a	1 articles
dry beriberi		A beriberi that is located_in the nervous system a..[+] A beriberi that is located_in the nervous system and has_symptom difficulty walking, numbness in extremities, tingling in extremities, paralysis of lower legs, difficulty speaking, confusion, and vomiting. [-]
dry eye syndrome	Tear film insufficiency; dry eye disease;	A lacrimal apparatus disease that is characterized..[+] A lacrimal apparatus disease that is characterized by persistent irritation or burning of the coreneal surface. [-]
ductal carcinoma in situ		n_a
dumping syndrome	Jejunal syndrome; Dumping (jejunal) syndrome;	n_a
duodenal atresia		An intestinal atresia that is characterized by con..[+] An intestinal atresia that is characterized by congenital absence or complete closure of a portion of the lumen of the duodenum. [-]
duodenal benign neoplasm	neoplasm of the duodenum; neoplasm of duodenum;	n_a
duodenal gastrinoma	Gastrinoma of duodenum; malignant duodenal gastrin.. [+] Gastrinoma of duodenum; malignant duodenal gastrinoma; duodenal G-cell gastrin producing tumor; [-]	n_a

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