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Disease	Synonyms	Description	Articles
acquired immunodeficiency syndrome	AIDS; acquired immune deficiency syndrome; acquire.. [+] AIDS; acquired immune deficiency syndrome; acquired Immune deficiency; [-]	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 microliter 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 laryngomalacia		A laryngeal disease that is characterized by acqui..[+] A laryngeal disease that is characterized by acquired collapse of laryngeal suprastructures. [-]
acquired metabolic disease		A disease of metabolism that has_material_basis_in..[+] 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. [-]	49 articles
acquired night blindness	acquired night blindness (disorder);	A nutritional deficiency disease that is character..[+] A nutritional deficiency disease that is characterized by vitamin A deficiency causing poor adaptation of the eyes to low levels of light, and has_material_basis_in lack of vitamin A such that rhodopsin, a light sensitive retinal pigment, cannot be regenerated. [-]
acquired polycythemia	secondary polycythemia; secondary polycythemia (di.. [+] secondary polycythemia; secondary polycythemia (disorder); secondary polycythemia NOS (disorder); Polycythemia, secondary; secondary Polycythemia; [-]	n_a
acquired tear duct stenosis	acquired nasolacrimal duct stenosis; Stenosis of n.. [+] acquired nasolacrimal duct stenosis; Stenosis of nasolacrimal duct, acquired; Tear duct - acquired stenosis; acquired stenosis of nasolacrimal duct; [-]	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; acral lentiginous melanoma, malignant; [-]	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. [-]
acrocallosal syndrome	ACLS; SCHINZEL ACROCALLOSAL SYNDROME; Schinzel syn.. [+] ACLS; SCHINZEL ACROCALLOSAL SYNDROME; Schinzel syndrome 1; [-]	A syndrome that is an autosomal recessive disorder..[+] A syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation. [-]
acrocapitofemoral dysplasia		An osteochondrodysplasia characterized by skeletal..[+] An osteochondrodysplasia characterized by skeletal dysplasia, bradydactyly and narrow thorax and has_material_basis_in mutations in the Indian hedgehog homolog gene. [-]
acrocardiofacial syndrome	cleft palate, cardiac defect, genital anomalies, a.. [+] cleft palate, cardiac defect, genital anomalies, and ectrodactyly; cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome; [-]	A syndrome characterized by split-hand/split-foot ..[+] A syndrome characterized by split-hand/split-foot malformation, facial anomalies, cleft lip/palate, congenital heart defect, genital anomalies, and intellectual deficit. [-]	1 articles
acrocephalosyndactylia	Apert syndrome;	A synostosis that results_in craniosynostosis and ..[+] A synostosis that results_in craniosynostosis and syndactyly. [-]	2 articles
acrodermatitis		A dermatitis that selectively affects the hands an..[+] A dermatitis that selectively affects the hands and feet. [-]
acrodermatitis chronica atrophicans	Herxheimer disease; primary diffuse atrophy;	An acrodermatitis characterized by a chronically p..[+] An acrodermatitis characterized by a chronically progressive course, leading to widespread atrophy of the skin. It is a clinical manifestation of Lyme borreliosis. [-]
acrodermatitis enteropathica		A metal metabolism disorder characterized by derma..[+] A metal metabolism disorder characterized by dermatitis around bodily openings and the tips of fingers and toes, alopecia and diarrhea and has_material_basis_in mutation in the SLC39A4 gene that encodes a zinc uptake protein and results in zinc deficiency. [-]
acrodysostosis		A dysostosis that results_in shortening of interph..[+] A dysostosis that results_in shortening of interphalangeal joints located_in hand or located_in foot along with mental deficiency. [-]
acrofacial dysostosis		n_a	5 articles
acrofacial dysostosis Cincinnati type		An acrofacial dysostosis characterized by a spectr..[+] An acrofacial dysostosis characterized by a spectrum of mandibulofacial dysostosis phenotypes, such as cleft palate, micrognathia, malar flattening, microcephaly and, in some cases, extrafacial skeletal defects. It is that has_material_basis_in heterozygous mutation in the POLR1A gene on chromosome 2p11. [-]
acrofacial dysostosis Rodriguez type	acrofacial dysostosis, syndrome of Rodriguez;	An acrofacial dysostosis that is characterized by ..[+] An acrofacial dysostosis that is characterized by CNS malformations, lung anomalies, congenital heart defects, dysmorphic facies and limb reduction, and has_material_basis_in autosomal recessive inheritance. [-]
acrofacial dysostosis, Catania type	Opitz Mollica Sorge syndrome; Opitz-Caltabiano syn.. [+] Opitz Mollica Sorge syndrome; Opitz-Caltabiano syndrome; [-]	An acrofacial dysostosis that is characterized by ..[+] An acrofacial dysostosis that is characterized by intrauterine growth retardation, short stature, microcephaly, cleft palate, limb hypoplasia, simian creases and cryptorchidism/hypospadias. [-]
acrofacial dysostosis, Patagonia type		An acrofacial dysostosis that is characterized by ..[+] An acrofacial dysostosis that is characterized by oligodontia, short stature, pili torti, syndactyly, vertebral abnormalities and cleft lip, and has_material_basis_in X-linked dominant inheritance. [-]
acrofrontofacionasal dysostosis	AFFN dysostosis; Richieri-Costa-Colletto syndrome;.. [+] AFFN dysostosis; Richieri-Costa-Colletto syndrome; [-]	A dysostosis characterized by intellectual disabil..[+] A dysostosis characterized by intellectual disability, short stature, hypertelorism, broad notched nasal tip, cleft lip palate, postaxial camptobrachypolysyndactyly, fibular hypoplasia and anomalies of foot structure. [-]
acrokeratosis verruciformis	Acrokeratosis verruciformis of Hopf; Hopf disease;.. [+] Acrokeratosis verruciformis of Hopf; Hopf disease; [-]	A keratosis that has_material_basis_in mutations i..[+] A keratosis that has_material_basis_in mutations in the ATP2A2 gene. [-]
acromegaly		A disease of metabolism that has_material_basis_in..[+] A disease of metabolism that has_material_basis_in excessive growth hormone production which results_in enlargement located_in limb. [-]
acromelic frontonasal dysostosis		A dysostosis characterized by cranium bifidum, sev..[+] A dysostosis characterized by cranium bifidum, severe hypertelorism, median cleft lip and palate, nasal bifurcation, brachycephaly, large fontanelle, tibial hemimelia, preaxial polydactyly of the feet and brain malformations. [-]
acromesomelic dysplasia		An osteochondrodysplasia that is characterized by ..[+] An osteochondrodysplasia that is characterized by mesomelia and acromelia, which results_in short limb dwarfism. [-]
acromesomelic dysplasia, Grebe type	GREBE CHONDRODYSPLASIA; acromesomelic dysplasia-2A.. [+] GREBE CHONDRODYSPLASIA; acromesomelic dysplasia-2A; grebe chondrodysplasia; [-]	An acromesomelic dysplasia that has_material_basis..[+] An acromesomelic dysplasia that has_material_basis_in mutation in CDMP-1 which results_in micromelia, absence of middle and proximal phalanges and some metacarpal and metatarsal bones. [-]
acromesomelic dysplasia, Hunter-Thompson type	acromesomelic dwarfism; acromesomelic dysplasia-2C.. [+] acromesomelic dwarfism; acromesomelic dysplasia-2C; [-]	An acromesomelic dysplasia that has_material_basis..[+] An acromesomelic dysplasia that has_material_basis_in mutation in AMDH gene which results_in normal axial skeleton but fused bones in the located_in hand or located_in foot. [-]
acromesomelic dysplasia, Maroteaux type	acromesomelic dysplasia-1;	An acromesomelic dysplasia that has_material_basis..[+] An acromesomelic dysplasia that has_material_basis_in mutation in NPR-B receptor which results_in severe dwarfism, abnormalities of the vertebral column and shortening of the limb middle and distal segments. [-]
acromesomelic dysplasia-3	Demirhan-type acromesomelic dysplasia;	An acromesomelic dysplasia that has_material_basis..[+] An acromesomelic dysplasia that has_material_basis_in homozygous mutation in the BMPR1B gene on chromosome 4q22. [-]
acromesomelic dysplasia-4		An acromesomelic dysplasia that is characterized b..[+] An acromesomelic dysplasia that is characterized by disproportionate short stature due to mesomelic shortening of the limbs and that has_material_basis_in homozygous mutation in the PRKG2 gene on chromosome 4q21. [-]
acromicric dysplasia	acromicric skeletal dysplasia; ACMICD;	An osteochondrodysplasia characterized by autosoma..[+] An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1. [-]
acrorenal syndrome		A syndrome characterized by limb defects, usually ..[+] A syndrome characterized by limb defects, usually bilateral, like cleft hands or feet and longitudinal defects involving radius or ulna, tibia or fibula and renal anomalies which include agenesis, hypoplasia and rarely polycystic kidneys. Additional malformations may involve the oro-mandibular region, the trachea and lungs, skin derivatives including sweat glands, mammary glands, the uterus, vas deferens, the nasal placodes and the eyes. [-]
actinic keratosis	actinic (Solar) Keratosis; Senile hyperkeratosis; .. [+] actinic (Solar) Keratosis; Senile hyperkeratosis; SK - Solar keratosis; Solar keratosis; [-]	n_a
actinobacillosis	Actinobacillosis, NOS; Actinobacillosis;	A commensal bacterial infectious disease that resu..[+] A commensal bacterial infectious disease that results_in infection, has_material_basis_in Actinobacillus ureae, which is a commensal of the human respiratory tract. The pathogen causes meningitis, endocarditis, bacteremia, atrophic rhinitis, bronchitis, pneumonia, conjunctivitis, peritonitis, and otitis media. [-]
actinomycosis	actinomycetoma; Actinomycotic madura foot (disorde.. [+] actinomycetoma; Actinomycotic madura foot (disorder); Actinomycotic mycetoma of foot; Madura foot due to Actinomadura (disorder); Actinomycotic madura foot; Madura foot due to Actinomadura; actinomycotic infection; Actinomycotic mycetema; boil; [-]	A commensal bacterial infectious disease that resu..[+] A commensal bacterial infectious disease that results in infection, which is characterized by contiguous spread, suppurative and granulomatous inflammation, and formation of multiple abscesses and sinus tracts that may discharge sulfur granules, has_material_basis_in Actinomyces israelii, has_material_basis_in Actinomyces gerencseriae, has_material_basis_in Actinomyces naeslundii, has_material_basis_in Actinomyces odontolyticus, has_material_basis_in Actinomyces viscosus, has_material_basis_in Actinomyces meyeri, has_material_basis_in Propionibacterium propionicum, which require a break in the integrity of the mucous membranes and the presence of devitalized tissue to invade deeper body structures. [-]
active cochlear Meniere's disease	active Meniere's disease, cochlear; Cochlear activ.. [+] active Meniere's disease, cochlear; Cochlear active Mnire's disease (disorder); active cochlear Meniere disease; Cochlear active Mnire's disease; [-]	n_a
active cochleovestibular Meniere's disease	Cochleovestibular active Mnire's disease (disorder.. [+] Cochleovestibular active Mnire's disease (disorder); active cochleovestibular Meniere disease; Cochleovestibular active Mnire's disease; active Meniere's disease, cochleovestibular; [-]	n_a
active peptic ulcer disease	GI Bleeding;	n_a
active vestibular Meniere's disease	active Meniere's disease, vestibular; active vesti.. [+] active Meniere's disease, vestibular; active vestibular Meniere disease; Vestibular active Mnire's disease (disorder); Vestibular active Mnire's disease; [-]	n_a
acute allergic mucoid otitis media		A blue drum syndrome caused by an allergen.
acute allergic sanguinous otitis media		A acute sanguinous otitis media caused by an aller..[+] A acute sanguinous otitis media caused by an allergen. [-]
acute allergic serous otitis media		A acute serous otitis media caused by an allergen.
acute anterolateral myocardial infarction		n_a
acute apical periodontitis	acute apical periodontitis of pulpal origin (disor.. [+] acute apical periodontitis of pulpal origin (disorder); acute apical periodontitis of pulpal origin; [-]	n_a
acute basophilic leukemia		An acute myeloid leukemia that is characterized by..[+] An acute myeloid leukemia that is characterized by primary differentiation to basophils. [-]
acute biphenotypic leukemia	B- and T-cell mixed leukemia; MPAL; mixed phenotyp.. [+] B- and T-cell mixed leukemia; MPAL; mixed phenotype acute leukemia; [-]	An acute leukemia that is characterized by the occ..[+] An acute leukemia that is characterized by the occurrence of more than one type of leukemia at the same time resulting from either the occurrence of blasts which coexpress myeloid and T or B lineage antigens or concurrent B and T lineage antigens. [-]
acute canaliculitis	acute canaliculitis, lacrimal; acute lacrimal cana.. [+] acute canaliculitis, lacrimal; acute lacrimal canaliculitis; [-]	An acute inflammation of lacrimal passage that is ..[+] An acute inflammation of lacrimal passage that is characterized by inflammation of the lacrimal caniculi, has_symptom epiphora, has_symptom conjunctivitis, has_symptom eyelid mattering and has_symptom purulent discharge. [-]
acute cervicitis		A cervicitis that is characterized by onset within..[+] A cervicitis that is characterized by onset within the past 1 - 3 days. [-]

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