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Disease	Synonyms	Description
abnormal retinal correspondence		n_a
abnormal threshold of rods	abnormal dark adaptation curve;	n_a
abnormality of glucagon secretion	Glucagon secretion abnormality;	n_a
absence epilepsy		An electroclinical syndrome characterized by the o..[+] An electroclinical syndrome characterized by the occurrence of generalized onset seizures that cause lapses in awareness, begin and end abruptly, typically last only a few seconds and are associated with abnormal spike-wave discharges as seen by electroencephalogram. [-]
acalculous cholecystitis	acute acalculous cholecystitis; acute cholecystiti.. [+] acute acalculous cholecystitis; acute cholecystitis without calculus (disorder); cholecystitis without calculus (disorder); acute cholecystitis without calculus; cholecystitis without calculus; [-]	A cholecystitis characterized by the absence of ga..[+] A cholecystitis characterized by the absence of gallstones. [-]
acanthocephaliasis		A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that involves infection of the intestine caused by thorny-headed worms Macracanthorhynchus or Moniliformis moniliformis. The infection has_symptom abdominal pain, has_symptom distension, has_symptom fever, has_symptom decreased appetite, has_symptom nausea, has_symptom vomiting, has_symptom weight loss, has_symptom diarrhea, and has_symptom constipation or has_symptom bloody stools. [-]
acantholytic acanthoma	Acantholytic acanthoma;	n_a
acantholytic squamous cell skin carcinoma	acantholytic squamous cell carcinoma of skin ; Aca.. [+] acantholytic squamous cell carcinoma of skin ; Acantholytic squamous cell carcinoma of skin (disorder); Acantholytic squamous cell skin carcinoma; [-]	n_a
acantholytic variant squamous cell breast carcinoma		n_a
acanthoma		n_a
acanthosis nigricans	Acanthosis nigricans (disorder); AN - Acanthosis n.. [+] Acanthosis nigricans (disorder); AN - Acanthosis nigricans; Keratosis nigricans; keratosis nigricans; [-]	A pigmentation disease characterized by velvety, d..[+] A pigmentation disease characterized by velvety, darkening of the skin usually in intertriginous areas. [-]
acatalasia	deficiency of catalase (disorder); acatalasemia; d.. [+] deficiency of catalase (disorder); acatalasemia; deficiency of catalase; [-]	A peroxisomal disease characterized by loss of cat..[+] A peroxisomal disease characterized by loss of catalase activity in erythrocytes that has_material_basis_in homozygous mutation in the CAT gene on chromosome 11p13. [-]
accessory nerve disease	disorder of 11th nerve; disorder of accessory [11t.. [+] disorder of 11th nerve; disorder of accessory [11th] nerve; disorder of accessory nerve (disorder); Eleventh nerve disorder; [-]	n_a
accommodative esotropia		n_a
accommodative spasm	Spasm of accommodation;	n_a
aceruloplasminemia		An iron metabolism disease that has_material_basis..[+] An iron metabolism disease that has_material_basis_in a mutation in the ceruloplasmin gene characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus. [-]
achalasia	achalasia of cardia; achalasia of esophagus; cardi.. [+] achalasia of cardia; achalasia of esophagus; cardiospasm; esophageal achalasia; hypertensive lower esophageal sphincter; Lack of reflex relaxation of lower oesophageal sphincter; [-]	An esophageal disease that is characterized by an ..[+] An esophageal disease that is characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing. [-]
achalasia microcephaly syndrome	Achalasia microcephaly; ACHALASIA-MICROCEPHALY SYN.. [+] Achalasia microcephaly; ACHALASIA-MICROCEPHALY SYNDROME; [-]	A syndrome that is characterized by microcephaly, ..[+] A syndrome that is characterized by microcephaly, intellectual deficit and early onset symptoms of achalasia (abnormal enlargement of the esophagus, impaired peristalsis, cardiospasm, recurrent vomiting and respiratory infections). [-]
acheiropody	Acheiropodia; Horn-Kolb Syndrome;	n_a
achondrogenesis		An osteochondrodysplasia that has_material_basis_i..[+] An osteochondrodysplasia that has_material_basis_in deficient endochondral ossification which results_in dwarfism, short-trunk, short-limbed, anascara, disproportionately large cranium, and a narrow chest which leads to death in utero or during early neonatal period. [-]
achondrogenesis type IA	achondrogenesis Houston-Harris type;	An achondrogenesis that results_in abnormal ossifi..[+] An achondrogenesis that results_in abnormal ossification of the located_in vertebral column or located_in spine. [-]
achondrogenesis type IB	achondrogenesis Fraccaro type;	An achondrogenesis that has_material_basis_in muta..[+] An achondrogenesis that has_material_basis_in mutation in the SLC26A2 gene which results_in umbilical or inguinal hernia and a prominent rounded abdomen. [-]
achondrogenesis type II		An achondrogenesis that has_material_basis_in muta..[+] An achondrogenesis that has_material_basis_in mutations in the COL2A1 gene which results_in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located_in vertebral column or located_in pelvis. [-]
achondroplasia	Achondroplastic physique; Chondrodystrophia; osteo.. [+] Achondroplastic physique; Chondrodystrophia; osteosclerosis congenita; [-]	An osteochondrodysplasia that results_in dwarfism ..[+] An osteochondrodysplasia that results_in dwarfism which has_material_basis_in abnormal ossification of cartilage in located_in long bone. [-]
achromatopsia	ACHM; Monochromatism;	A color blindness that is characterized by a conge..[+] A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. [-]
achromatopsia 2	ACHM2; RMCH2; rod monochromacy 2; rod monochromati.. [+] ACHM2; RMCH2; rod monochromacy 2; rod monochromatism 2; [-]	An achromatopsia that has_material_basis_in homozy..[+] An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGA3 gene on chromosome 2q11. [-]
achromatopsia 3	ACHM1; ACHM3; Pingelapese blindness; RMCH1; rod mo.. [+] ACHM1; ACHM3; Pingelapese blindness; RMCH1; rod monochromacy 1; rod monochromatism 1; [-]	An achromatopsia that has_material_basis_in homozy..[+] An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the CNGB3 gene on chromosome 8q2. [-]
achromatopsia 4	ACHM4;	An achromatopsia that has material basis in homozy..[+] An achromatopsia that has material basis in homozygous or compound heterozygous mutation in the GNAT2 gene (139340) on chromosome 1p13. [-]
achromatopsia 7	ACHM7;	An achromatopsia that has_material_basis_in homozy..[+] An achromatopsia that has_material_basis_in homozygous or compound heterozygous mutation in the ATF6 gene on chromosome 1q23. [-]
acidophil adenoma	Eosinophil adenoma;	n_a
acinar cell carcinoma	acinar cell carcinoma (morphologic abnormality); a.. [+] acinar cell carcinoma (morphologic abnormality); acinic cell carcinoma; [-]	A carcinoma that has_material_basis_in abnormally ..[+] A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from spindle cells and/or derives_from giant cells. [-]
acinar cell cystadenocarcinoma	acinar cell cystadenocarcinoma (morphologic abnorm.. [+] acinar cell cystadenocarcinoma (morphologic abnormality); pancreatic acinar cell cystadenocarcinoma; [-]	n_a
acinic cell breast carcinoma		A breast adenocarcinoma that is characterized by w..[+] A breast adenocarcinoma that is characterized by widespread acinar cell-like differentiation. [-]
acne	Acne varioliformis; acne vulgaris; frontalis acne;.. [+] Acne varioliformis; acne vulgaris; frontalis acne; [-]	A sebaceous gland disease characterized by areas o..[+] A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring. [-]
acneiform dermatitis		n_a
acoustic neuroma	Vestibular Neurilemmoma; Vestibular schwannoma;	n_a
acquired angioedema		An angioedema that is characterized by an acquired..[+] An angioedema that is characterized by an acquired deficiency of (C1-INH) caused by either consumption or inactivation. [-]
acquired color blindness	acquired color vision deficiencies; acquired color.. [+] acquired color vision deficiencies; acquired color vision deficiency; [-]	n_a
acquired gastric outlet stenosis	acquired hypertrophic pyloric stenosis; adult hype.. [+] acquired hypertrophic pyloric stenosis; adult hypertrophic pyloric stenosis; [-]	n_a
acquired generalized lipodystrophy	Lawrence syndrome;	A complete generalized lipodystrophy that is charc..[+] A complete generalized lipodystrophy that is charcterized by generalized disappearance of fat occurring during childhood and adolescence where normal body fat is present at birth. [-]
acquired hemangioma		n_a
acquired hyperkeratosis	acquired Keratoderma; acquired keratoderma; acquir.. [+] acquired Keratoderma; acquired keratoderma; acquired keratoderma (disorder); acquired keratoderma NOS; acquired keratoderma NOS (disorder); Keratoderma - acquired; Keratoderma, acquired; [-]	n_a
acquired immunodeficiency syndrome	acquired Immune deficiency; acquired immune defici.. [+] acquired Immune deficiency; acquired immune deficiency syndrome; AIDS; [-]	A Human immunodeficiency virus infectious disease ..[+] A Human immunodeficiency virus infectious disease that results_in reduction in the numbers of CD4-bearing helper T cells below 200 per ÂµL of blood or 14% of all lymphocytes thereby rendering the subject highly vulnerable to life-threatening infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted_by sexual contact, transmitted_by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted_by congenital method, and transmitted_by contaminated needles. Opportunistic infections are common in people with AIDS. [-]
acquired metabolic disease		A disease of metabolism that has _material_basis_i..[+] A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or malabsorption. [-]
acquired night blindness	acquired night blindness (disorder);	n_a
acquired polycythemia	Polycythemia, secondary; secondary Polycythemia; s.. [+] Polycythemia, secondary; secondary Polycythemia; secondary polycythemia; secondary polycythemia (disorder); secondary polycythemia NOS (disorder); [-]	n_a
acquired tear duct stenosis	acquired nasolacrimal duct stenosis; acquired sten.. [+] acquired nasolacrimal duct stenosis; acquired stenosis of nasolacrimal duct; Stenosis of nasolacrimal duct, acquired; Tear duct - acquired stenosis; [-]	n_a
acquired thrombocytopenia	acquired thrombocytopenia (disorder); secondary th.. [+] acquired thrombocytopenia (disorder); secondary thrombocytopenia; secondary thrombocytopenia NOS; secondary thrombocytopenia NOS (disorder); [-]	n_a
acquired von Willebrand syndrome	AVWS;	A blood coagulation disease characterized by devel..[+] A blood coagulation disease characterized by development of a defect in clotting in the absence of previous bleeding symptoms, negative familial history, and occurrence in a relatively older age. Typically this develops secondarily to other disorders, such as lymphoproliferative, myeloproliferative, cardiovascular and autoimmune disorders. [-]
acral lentiginous melanoma	acral lentiginous melanoma, malignant (morphologic.. [+] acral lentiginous melanoma, malignant (morphologic abnormality); malignant acral lentiginous melanoma; [-]	A skin melanoma that is characterized by slow grow..[+] A skin melanoma that is characterized by slow growth of a small pigmented spot on the skin with a clearly defined edge, surrounded by normal-appearing skin and occurs on occurs on non hair-bairing surfaces including hands and feet, subungual sites, and fingers or toes. [-]

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