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Disease	Synonyms	Description
basal cell carcinoma	Basal cell carcinoma NOS (morphologic abnormality).. [+] Basal cell carcinoma NOS (morphologic abnormality); BASAL CELL carcinoma OF SKIN; Basal cell carcinoma of skin (disorder); Basal cell neoplasm (morphologic abnormality); Basal cell neoplasm NOS (morphologic abnormality); Basal cell tumor (morphologic abnormality); Basal cell cancer; Basal cell tumor; Epithelioma basal cell (disorder); malignant basal cell tumor (morphologic abnormality); Rodent ulcer; Basal cell carcinoma of skin; Basal cell neoplasm; Epithelioma basal cell; malignant Basal cell neoplasm; malignant basal cell tumor; [-]	A skin carcinoma affecting basal cells.
basal ganglia calcification	Fahr disease;	A basal ganglia disease characterized by the prese..[+] A basal ganglia disease characterized by the presence of abnormal calcium deposits of unknown cause in the brain; has symptom dementia, psychosis, mood swings and loss of acquired motor skills. [-]
basal ganglia cerebrovascular disease		n_a
basal ganglia disease		A brain disease that is characterized by dysfuncti..[+] A brain disease that is characterized by dysfunctional movement, located_in basal ganglia that has_material_basis_in diseased components of the basal ganglia and associated neural circuits. [-]
basal laminar drusen	cuticular drusen; drusen of bruch membrane; early .. [+] cuticular drusen; drusen of bruch membrane; early adult-onset grouped drusen; [-]	A retinal drusen characterized by yellow-white dep..[+] A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has_material_basis_in mutations in the CFH gene on chromosome 1q31.3. [-]
basaloid lung carcinoma		n_a
basaloid squamous cell carcinoma	Basaloid carcinoma (morphologic abnormality); Basa.. [+] Basaloid carcinoma (morphologic abnormality); Basaloid squamous cell carcinoma (morphologic abnormality); Basaloid carcinoma; [-]	A squamous cell carcinoma that has a solid, closel..[+] A squamous cell carcinoma that has a solid, closely packed growth of cells with hyperchromatic nuclei, scant cytoplasm, small cystic spaces, and foci of necrosis. It has overlying squamous dysplasia, rare foci of overt keratinization, and/or coexistent keratinizing squamous cell carcinoma. [-]
basaloid squamous cell skin carcinoma	skin Basaloid squamous cell carcinoma;	n_a
BASAN syndrome		An ectodermal dysplasia that is characterized by n..[+] An ectodermal dysplasia that is characterized by neonatal blisters and milia and congenital absence of dermatoglyphics on the hands and feet. [-]
basidiobolomycosis		A subcutaneous mycosis that involves a chronic inf..[+] A subcutaneous mycosis that involves a chronic inflammatory or granulomatous fungal infection of the subcutaneous tissue of the limbs, chest, back or buttocks caused by Basidiobolus ranarum. Lesions appear as subcutaneous nodules which develop into massive, firm, indurated, painless swellings which are freely movable over the underlying muscle, but are attached to the skin which may become hyperpigmented but not ulcerated. [-]
basilar artery insufficiency	Basilar artery syndrome (disorder); Basilar artery.. [+] Basilar artery syndrome (disorder); Basilar artery syndrome; [-]	n_a
basilar artery occlusion		n_a
Basilicata-Akhtar syndrome	MRXS36; X-linked syndromic mental retardation 36; .. [+] MRXS36; X-linked syndromic mental retardation 36; X-linked syndromic mental retardation Basilicata-Akhtar type; [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by global developmental delay apparent from infancy, feeding difficulties, hypotonia, and poor or absent speech that has_material_basis_in hemizygous or heterozygous mutation in the MSL3 gene on chromosome Xp22.2. [-]
basophil adenoma	Pituitary gland Basophilic adenoma;	n_a
basophilic adenocarcinoma	Basophil carcinoma (morphologic abnormality); Baso.. [+] Basophil carcinoma (morphologic abnormality); Basophil adenocarcinoma; Basophil carcinoma; basophilic carcinoma; [-]	n_a
basosquamous carcinoma	Metatypical carcinoma (morphologic abnormality); B.. [+] Metatypical carcinoma (morphologic abnormality); Basisquamous cell carcinoma; basosquamous cell carcinoma; Metatypical carcinoma; [-]	n_a
baylisascariasis		A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that involves parasitic infection of the intestine caused by the larvae of Baylisascaris procyonis, which can invade the spinal cord, brain, and eye of humans, resulting in permanent neurologic damage, blindness, or death. [-]
B-cell acute lymphoblastic leukemia	B acute lymphoblastic leukemia; B-cell acute lymph.. [+] B acute lymphoblastic leukemia; B-cell acute lymphocytic leukemia; [-]	An acute lymphocytic leukemia characterized by too..[+] An acute lymphocytic leukemia characterized by too many B-cell lymphoblasts (immature white blood cells) in the bone marrow and blood. [-]
B-cell adult acute lymphocytic leukemia	adult B acute lymphoblastic leukemia; adult b-cell.. [+] adult B acute lymphoblastic leukemia; adult b-cell acute lymphoblastic leukemia; adult b-cell lymphocytic leukemia; adult B-lymphoblastic leukemia; adult B acute lymphoblastic leukaemia; adult b-cell acute lymphoblastic leukaemia; adult b-cell lymphocytic leukaemia; adult B-lymphoblastic leukaemia; B-cell adult acute lymphocytic leukaemia; [-]	An adult acute lymphoblastic leukemia occurring in..[+] An adult acute lymphoblastic leukemia occurring in adults and that has_material_basis_in B lymphocytes. [-]
B cell and dendritic cell deficiency		A combined immunodeficiency characterized by impai..[+] A combined immunodeficiency characterized by impaired function or reduced numbers of dendritic cells and B cells. [-]
B cell deficiency	Immunoglobulin heavy chain deficiency (disorder); .. [+] Immunoglobulin heavy chain deficiency (disorder); B cell (antibody) deficiencies; immunoglobulin heavy chain deletion; Immunoglobulin heavy chain deficiency; [-]	A primary immunnodeficiency disease that is caused..[+] A primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly. [-]
B-cell lymphoma	B-cell lymphocytic neoplasm;	A non-Hodgkin lymphoma that has_material_basis_in ..[+] A non-Hodgkin lymphoma that has_material_basis_in B cells. [-]
B-cell prolymphocytic leukemia	B Cell Prolymphocytic Leukemia; Prolymphocytic leu.. [+] B Cell Prolymphocytic Leukemia; Prolymphocytic leukemia, B-cell type; [-]	A prolymphocytic leukemia that is characterized by..[+] A prolymphocytic leukemia that is characterized by medium-sized, round lymphoid cells with prominent nucleoli exceeding 55% of lymphoid cells in the blood. [-]
BCOR-CCNB3 sarcoma		A sarcoma with BCOR genetic alterations that is ch..[+] A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR-CCNB3 fusion gene. [-]
BCOR ITD sarcoma		A sarcoma with BCOR genetic alterations that is ch..[+] A sarcoma with BCOR genetic alterations that is characterized by the presence of BCOR internal tandem duplication. [-]
beach ear	acute bacterial inflammation of external ear (diso.. [+] acute bacterial inflammation of external ear (disorder); acute swimmer's ear (disorder); acute swimmer's ear; acute swimmers' ear; Tank ear; acute bacterial inflammation of external ear; acute otitis externa, diffuse; [-]	An otitis externa which is a microbial infection t..[+] An otitis externa which is a microbial infection that occurs suddenly, rapidly worsens, and becomes very painful and alarming. It is caused by swimming in polluted water, scratching the ear or inside the ear and object stuck in the ear. It is occasionally associated with middle ear infection or upper respiratory infections such as colds. [-]
Beare-Stevenson cutis gyrata syndrome		A syndrome that is characterized by cutis gyrata, ..[+] A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26. [-]
Becker disease		A myotonia congenita that is characterized by musc..[+] A myotonia congenita that is characterized by muscle stiffness and an inability of the muscle to relax after voluntary contraction and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding skeletal muscle chloride channel-1 (CLCN1) on chromosome 7q34. [-]
Becker muscular dystrophy	benign congenital myopathy; Benign pseudohypertrop.. [+] benign congenital myopathy; Benign pseudohypertrophic muscular dystrophy; [-]	A muscular dystrophy that involves slowly worsenin..[+] A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21. [-]
Beckwith-Wiedemann syndrome		A syndrome characterized by overgrowth (macrosomia..[+] A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. [-]
Beemer-Langer syndrome	type IV short rib polydactyly syndrome (disorder);.. [+] type IV short rib polydactyly syndrome (disorder); type IV short rib polydactyly syndrome; [-]	A syndrome that results_in multiple congenital ano..[+] A syndrome that results_in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly. [-]
Behcet's disease	Adamantiades-Behcet disease; Behcet syndrome; Behc.. [+] Adamantiades-Behcet disease; Behcet syndrome; Behcet's syndrome; Behet's syndrome; triple symptom complex; [-]	A vasculitis that is characterized by an autoimmun..[+] A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. [-]
Behcet's syndrome arthropathy	Arthropathy in Behcet's syndrome involving ankle a.. [+] Arthropathy in Behcet's syndrome involving ankle and foot; Arthropathy in Behcet's syndrome involving forearm; Arthropathy in Behcet's syndrome involving hand; Arthropathy in Behcet's syndrome involving lower leg; Arthropathy in Behcet's syndrome involving multiple sites; Arthropathy in Behcet's syndrome involving pelvic region and thigh; Arthropathy in Behcet's syndrome involving shoulder region; Arthropathy in Behcet's syndrome involving upper arm; Behcet syndrome arthropathy; [-]	n_a
Behr syndrome	Abortive cerebellar ataxia (BEHRS); BEHRS; optic a.. [+] Abortive cerebellar ataxia (BEHRS); BEHRS; optic atrophy, infantile hereditary, Behr complicated form of; optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss; [-]	A nervous system disease characterized by early-on..[+] A nervous system disease characterized by early-onset optic atrophy, ataxia, pyramidal signs, spasticity, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the OPA1 gene on chromosome 3q29. [-]
bejel	Njovera; Nonvenereal endemic syphilis;	A primary bacterial infectious disease that result..[+] A primary bacterial infectious disease that results in infection located in mucosa of mouth, located in skin or located in bone, has_material_basis_in Treponema pallidum subsp endemicum, which is transmitted by contact or transmitted by sharing of domestic utensils. The infection has symptom moist patches in the mouth, has symptom lumps in long bones, tissues around the mouth, nose, and roof of the mouth. These lumps destroy tissue, causing bones to be deformed and disfiguring the face. [-]
Bell's palsy	Bell palsy; Bell's (facial) palsy;	A facial paralysis resulting from dysfunction in t..[+] A facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve). [-]
benign breast adenomyoepithelioma	benign Adenomyoepithelioma of the breast;	A breast benign neoplasm that is characterized by ..[+] A breast benign neoplasm that is characterized by dual differentiation into luminal cells and myoepithelial cells. [-]
benign breast phyllodes tumor	Cystosarcoma phyllodes NOS (morphologic abnormalit.. [+] Cystosarcoma phyllodes NOS (morphologic abnormality); Cystosarcoma phyllodes, NOS; Phyllodes tumor, benign (morphologic abnormality); benign cystosarcoma phyllodes; benign Phyllodes neoplasm; benign Phyllodes neoplasm of the breast; Cystosarcoma phyllodes; Phyllodes neoplasm; [-]	A breast benign neoplasm that has_material_basis_i..[+] A breast benign neoplasm that has_material_basis_in epithelial and stromal tissue and derives_from periductal stromal cells of the breast. [-]
benign deep fibrous histiocytoma		n_a
benign dermal neurilemmoma	benign Schwannoma of the skin;	n_a
benign eccrine breast spiradenoma	benign Eccrine breast Spiradenoma;	A breast benign neoplasm that arises_from cutaneou..[+] A breast benign neoplasm that arises_from cutaneous sweat glands and is characterized microscopically by two-cell populations: small, dark, basaloid cells with hyperchromatic nuclei, which are immunoreactive for P63 and calponin, and larger cells with a pale nucleus, often near the center of the cluster (inner cells), which are immunoreactive for CK7 and CD117 (C-kit). [-]
benign ependymoma	epithelial ependymoma; WHO grade II Ependymal tumo.. [+] epithelial ependymoma; WHO grade II Ependymal tumor; [-]	n_a
benign epilepsy with centrotemporal spikes	sylvan seizures ; BCECTS; benign childhood epileps.. [+] sylvan seizures ; BCECTS; benign childhood epilepsy with centrotemporal spike; benign Rolandic epilepsy; rolandic epilepsy; sylvan seizures; [-]	A childhood electroclinical syndrome characterized..[+] A childhood electroclinical syndrome characterized by partial seizures involving the rolandic area of the brain and electroencephalographic centrotemporal sharp waves. [-]
benign essential hypertension	benign Essential hypertension; benign essential hy.. [+] benign Essential hypertension; benign essential hypertension (disorder); [-]	n_a
benign exocrine pancreas neoplasm		An endocrine organ benign neoplasm arising from th..[+] An endocrine organ benign neoplasm arising from the exocrine pancreas. [-]
benign familial hematuria	BFH; thin basement membrane nephropathy; thin memb.. [+] BFH; thin basement membrane nephropathy; thin membrane nephropathy; TMN; [-]	A urinary system disease characterized by the pres..[+] A urinary system disease characterized by the presence of blood in the urine, thinning of the glomerular basement membrane and normal renal function that has_material_basis_in heterozygous mutation in the COL4A3 gene or the COL4A4 gene on chromosome 2q36.3. [-]
benign familial infantile epilepsy	BFIE ; benign familial infantile convulsion; benig.. [+] BFIE ; benign familial infantile convulsion; benign familial infantile seizures; BFIC; BFIE; [-]	An infancy electroclinical syndrome that is charac..[+] An infancy electroclinical syndrome that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae. [-]
benign familial infantile seizures 1	Benign Familial Infantile Seizures, 1;	A benign familial infantile epilepsy that is chara..[+] A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in the BFIS1 locus mapped to chromosome 19q. [-]
benign familial infantile seizures 2	Benign Familial Infantile Seizures, 2;	A benign familial infantile epilepsy that is chara..[+] A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutation in the PRRT2 gene on chromosome 16p11. [-]
benign familial infantile seizures 3	Benign Familial Infantile Seizures, 3; benign fami.. [+] Benign Familial Infantile Seizures, 3; benign familial neonatal-infantile seizures; [-]	A benign familial infantile epilepsy that is chara..[+] A benign familial infantile epilepsy that is characterized by afebrile partial complex or generalized tonic-clonic seizures occurring between 3 and 12 months of age with a good response to medication and no neurologic sequelae and that has_material_basis_in mutations in the SCN2A gene on chromosome 2q24. [-]

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