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Disease	Synonyms	Description	Articles
facial neuralgia		n_a
facial paralysis	Facial Palsy;	n_a
facioscapulohumeral muscular dystrophy	Landouzy Dejerine muscular dystrophy; Muscular dys.. [+] Landouzy Dejerine muscular dystrophy; Muscular dystrophy, Landouzy-Dejerine; Landouzy-Dejerine muscular dystrophy; [-]	n_a	2 articles
facioscapulohumeral muscular dystrophy 1	facioscapulohumeral muscular dystrophy type 1; fac.. [+] facioscapulohumeral muscular dystrophy type 1; facioscapulohumeral muscular dystrophy type 1A; FSHD1; [-]	A facioscapulohumeral muscular dystrophy that has_..[+] A facioscapulohumeral muscular dystrophy that has_material_basis_in contraction of the D4Z4 macrosatellite repeat in the subtelomeric region of chromosome 4q35. [-]
facioscapulohumeral muscular dystrophy 2	facioscapulohumeral muscular dystrophy 1B; faciosc.. [+] facioscapulohumeral muscular dystrophy 1B; facioscapulohumeral muscular dystrophy type 2; FSHD2; [-]	A facioscapulohumeral muscular dystrophy that has_..[+] A facioscapulohumeral muscular dystrophy that has_material_basis_in digenic inheritance of a heterozygous mutation in the SMCHDI gene on 18p11.32 and a haplotype on chromosome 4 that is permissive for DUX4 expression. [-]
facioscapulohumeral muscular dystrophy 3	facioscapulohumeral muscular dystrophy type 3; FSH.. [+] facioscapulohumeral muscular dystrophy type 3; FSHD3; [-]	A facioscapulohumeral muscular dystrophy character..[+] A facioscapulohumeral muscular dystrophy characterized by adult onset of proximal muscle weakness affecting the face, neck, scapular muscles, and upper and lower limbs that has_material_basis_in the combination of a homozygous mutation in the LRIF1 gene on chromosome 1p13 and presence of a haplotype on chromosome 4 that is permissive for DUX4 expression. [-]
facioscapulohumeral muscular dystrophy 4	facioscapulohumeral muscular dystrophy type 4; FSH.. [+] facioscapulohumeral muscular dystrophy type 4; FSHD4; [-]	A facioscapulohumeral muscular dystrophy character..[+] A facioscapulohumeral muscular dystrophy characterized by adult onset of progressive muscle weakness of the face and upper extremity muscles with disease progression that has_material_basis_in the combination of a heterozygous mutation in the DNMT3B gene on chromosome 20q11 and presence of a haplotype on chromosome 4 that is permissive for DUX4 expression. [-]
factitious disorder	Munchausen syndrome ;	A disease of mental health where symptoms are deli..[+] A disease of mental health where symptoms are deliberately produced, feigned or exaggerated in order to falsely demonstrate the presence of an illness. [-]
factor V deficiency	deficiency, labile; Hereditary hypoproaccelerinaem.. [+] deficiency, labile; Hereditary hypoproaccelerinaemia; Labile factor deficiency; Proaccelerin deficiency; [-]	n_a
factor VII deficiency	deficiency, stable; Factor VII deficiency; Factor .. [+] deficiency, stable; Factor VII deficiency; Factor VII deficiency (disorder); [-]	A blood coagulation disease that is characterized ..[+] A blood coagulation disease that is characterized by easy bleeding, has_symptom epistaxis, bleeding of the gums, menorrhagia, and occasionally hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation in the F7 gene, which encodes coagulation factor VII, an important factor in the clotting cascade. [-]
factor VIII deficiency	Subhemophilia; Congenital factor VIII disorder; cl.. [+] Subhemophilia; Congenital factor VIII disorder; classic hemophilia A; Hemophilia A; [-]	A blood coagulation disease that has_material_basi..[+] A blood coagulation disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged. [-]
factor X deficiency	disease, Stuart-Prower; Factor X deficiency (disor.. [+] disease, Stuart-Prower; Factor X deficiency (disorder); Factor X deficiency; [-]	A blood coagulation disease that is characterized ..[+] A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood. [-]
factor XI deficiency	Hereditary factor XI deficiency disease; plasma th.. [+] Hereditary factor XI deficiency disease; plasma thromboplastin antecedent deficiency; Rosenthal's disease; Congenital factor XI deficiency; hemophilia C; [-]	A blood coagulation disease that is characterized ..[+] A blood coagulation disease that is characterized by deficiency of factor XI clotting factor and mild prolonged bleeding, especially of mucosal sites following trauma, and has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation of the coagulation factor XI gene of chromosome 4q35.2. [-]
factor XII deficiency	deficiency, Hageman; Hageman Factor deficiency; Fa.. [+] deficiency, Hageman; Hageman Factor deficiency; Factor XII deficiency disease; [-]	A blood coagulation disease that is characterized ..[+] A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33. [-]
factor XIII deficiency	Factor XIII deficiency disease (disorder); Heredit.. [+] Factor XIII deficiency disease (disorder); Hereditary factor XIII deficiency disease (disorder); Factor XIII deficiency disease; Hereditary factor XIII deficiency disease; deficiency, Laki-Lorand factor; [-]	A blood coagulation disease that is characterized ..[+] A blood coagulation disease that is characterized by easy bleeding, has_symptom prolonged umbilical cord bleeding, epistaxis, bleeding of the gums, menorrhagia, recurrent miscarriages, abnormal scar formation and wound healing, and hemarthrosis, and has_material_basis_in autosomal recessive inheritance of mutation of the F13A1 or F13B gene, which encodes Factor XIII, formally known as fibrin stabilizing factor. [-]
fallopian tube adenocarcinoma	adenocarcinoma of the fallopian tube;	A fallopian tube carcinoma that derives_from epith..[+] A fallopian tube carcinoma that derives_from epithelial cells of glandular origin. [-]
fallopian tube adenofibroma		n_a
fallopian tube adenomatoid tumor		n_a
fallopian tube adenosarcoma	fallopian tube mullerian adenosarcoma;	n_a
fallopian tube benign neoplasm		n_a
fallopian tube cancer	malignant neoplasm of uterine tube; malignant tumo.. [+] malignant neoplasm of uterine tube; malignant tumour of fallopian tube; neoplasm of fallopian tube (disorder); tumor of the fallopian tube; tumor, fallopian tube, malignant; malignant tumor of fallopian tube (disorder); malignant tumor of fallopian tube; neoplasm of fallopian tube; fallopian tube neoplasm; [-]	A female reproductive organ cancer that is located..[+] A female reproductive organ cancer that is located_in fallopian tube. [-]
fallopian tube carcinoma	cancer of the fallopian tube; carcinoma of fallopi.. [+] cancer of the fallopian tube; carcinoma of fallopian tube (disorder); fallopian tube Ca; carcinoma of fallopian tube; [-]	A fallopian tube cancer that is located_in the fal..[+] A fallopian tube cancer that is located_in the fallopian tube. [-]
fallopian tube carcinosarcoma	fallopian tube malignant mixed Mullerian tumor; fa.. [+] fallopian tube malignant mixed Mullerian tumor; fallopian tube malignant mixed mesodermal (mullerian) tumor; [-]	A fallopian tube cancer that is characterized as a..[+] A fallopian tube cancer that is characterized as a mixture of carcinoma and sarcoma and has_material_basis_in epithelial tissue and has_material_basis_in connective tissue. [-]
fallopian tube clear cell adenocarcinoma	Clear cell carcinoma of the fallopian tube;	A fallopian tube adenocarcinoma that derives_from ..[+] A fallopian tube adenocarcinoma that derives_from epithelial cells which have clear cytoplasm. [-]
fallopian tube cystadenofibroma		n_a
fallopian tube disease		A female reproductive system disease that is locat..[+] A female reproductive system disease that is located_in the fallopian tube. [-]
fallopian tube endometrioid adenocarcinoma	endometrioid carcinoma of the fallopian tube; fall.. [+] endometrioid carcinoma of the fallopian tube; fallopian tube endometrioid cancer; fallopian tube endometrioid neoplasm; [-]	n_a
fallopian tube endometriosis	Endometriosis of fallopian tube;	A female reproductive system disease characterized..[+] A female reproductive system disease characterized by the growth of endometrial tissue that is located_in the fallopian tube. [-]
fallopian tube germ cell cancer	fallopian tube germ cell neoplasm;	n_a
fallopian tube gestational choriocarcinoma	Gestational Choriocarcinoma of the fallopian tube;.. [+] Gestational Choriocarcinoma of the fallopian tube; [-]	A gestational choriocarcinoma that is located_in t..[+] A gestational choriocarcinoma that is located_in the fallopian tube. [-]
fallopian tube leiomyoma		A fallopian tube benign neoplasm that has_material..[+] A fallopian tube benign neoplasm that has_material_basis_in smooth muscle cells. [-]
fallopian tube leiomyosarcoma		n_a
fallopian tube mucinous adenocarcinoma		A fallopian tube adenocarcinoma that derives_from ..[+] A fallopian tube adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin. [-]
fallopian tube mucinous tumor		A fallopian tube benign neoplasm that produces muc..[+] A fallopian tube benign neoplasm that produces mucin. [-]
fallopian tube papillary adenocarcinoma	Papillary adenocarcinoma of the fallopian tube;	n_a
fallopian tube serous adenocarcinoma		n_a
fallopian tube serous papilloma		n_a
fallopian tube squamous cell carcinoma	squamous cell carcinoma of the fallopian tube;	A fallopian tube carcinoma that derives_from squam..[+] A fallopian tube carcinoma that derives_from squamous epithelial cells. [-]
fallopian tube teratoma		n_a
fallopian tube transitional cell carcinoma		A fallopian tube carcinoma that derives_from epith..[+] A fallopian tube carcinoma that derives_from epithelial transitional cells. [-]
familial Behcet-like autoinflammatory syndrome	A20 haploinsufficiency;	A primary immunodeficiency disease that is charact..[+] A primary immunodeficiency disease that is characterized by characterized by ulceration of mucosal surfaces, particularly in the oral and genital areas and that has_material_basis_in heterozygous mutation in the TNFAIP3 gene on chromosome 6q23. [-]
familial GPIHBP1 deficiency	familial glycosylphosphatidylinositol-anchored hig.. [+] familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency; hyperlipoproteinemia type 1D; hyperlipoproteinemia type ID; [-]	A familial chylomicronemia syndrome characterized ..[+] A familial chylomicronemia syndrome characterized by refactory fasting hyperchylomicronemia, and elevated plasma triglyceride levels that has_material_basis_in homozygous or compound heterozygous mutation in the GPIHBP1 gene on chromosome 8q24.3. [-]
familial Mediterranean fever	benign paroxysmal peritonitis; FMF;	An autoimmune disease characterized by recurrent e..[+] An autoimmune disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; that has_material_basis_in mutations in the MEFV gene, which encodes the protein pyrin. [-]
familial adenomatous polyposis	adenomatous polyposis of the colon;	An intestinal disease that has_material_basis_in m..[+] An intestinal disease that has_material_basis_in mutations in the APC gene and involves formation of numerous polyps in the epithelium of the large intestine which are initially benign and later transform into colon cancer. [-]	3 articles
familial adenomatous polyposis 1		A familial adenomatous polyposis that has_material..[+] A familial adenomatous polyposis that has_material_basis_in heterozygous mutation in the APC gene on chromosome 5q22. [-]
familial adenomatous polyposis 2	MUTYH-related attenuated familial adenomatous poly.. [+] MUTYH-related attenuated familial adenomatous polyposis; MUTYH-related attenuated familial polyposis coli; MUTYH-related attenuated FAP; MUTYH-associated polyposis; [-]	A familial adenomatous polyposis that has_material..[+] A familial adenomatous polyposis that has_material_basis_in homozygous or compound heterozygous mutation in the MUTYH gene on chromosome 1p34. [-]
familial adenomatous polyposis 3		A familial adenomatous polyposis that has_material..[+] A familial adenomatous polyposis that has_material_basis_in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13. [-]
familial adenomatous polyposis 4		A familial adenomatous polyposis characterized by ..[+] A familial adenomatous polyposis characterized by the development of multiple colonic adenomas in adulthood, often with progression to colorectal cancer and that has_material_basis_in compound heterozygous mutation in the MSH3 gene on chromosome 5q11. [-]
familial adult myoclonic epilepsy	BAFME; benign adult familial myoclonus epilepsy; f.. [+] BAFME; benign adult familial myoclonus epilepsy; familial cortical myoclonic tremor and epilepsy; FAME; FCMTE; benign adult familial myoclonic epilepsy; [-]	An adolescence-adult electroclinical syndrome char..[+] An adolescence-adult electroclinical syndrome characterized by adult-onset cortical myoclonus typically first seen as tremulous finger movements and myoclonus of the extremities. [-]
familial adult myoclonic epilepsy 1	benign adult familial myoclonic epilepsy 1; FAME1;.. [+] benign adult familial myoclonic epilepsy 1; FAME1; FCMTE1; BAFME1; familial cortical myoclonic tremor and epilepsy 1; [-]	A familial adult myoclonic epilepsy that has_mater..[+] A familial adult myoclonic epilepsy that has_material_basis_in a heterozygous 5-bp repeat expansion in the SAMD12 gene on chromosome 8q24.11-q24.12. [-]

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