Xenbase

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Results 1 - 15 of 15 results

Page(s): 1

Disease	Synonyms	Description	Articles	Phenotypes
Queensland tick typhus	Queensland tick typhus (disorder); Australian tick.. [+] Queensland tick typhus (disorder); Australian tick typhus; Rickettsia australis spotted fever; North Queensland tick typhus [-]	A spotted fever that has_material_basis_in Rickett..[+] A spotted fever that has_material_basis_in Rickettsia australis, which is transmitted_by ticks (Ixodes holocyclus). The infection has_symptom fever, has_symptom headache, has_symptom myalgia, has_symptom maculopapular rash, and has_symptom lymphadenopathy. [-]
Q fever	Infection due to Coxiella burnetii (disorder); Inf.. [+] Infection due to Coxiella burnetii (disorder); Infection due to Coxiella burnetii [-]	A primary bacterial infectious disease that is a z..[+] A primary bacterial infectious disease that is a zoonotic infectious disease affecting multiple organs, has_material_basis_in Coxiella burnetii, which is transmitted_by inhalation of air contaminated by barnyard dust containing dried placental material, birth fluids, or excreta of infected herd animals, transmitted_by ingestion of contaminated milk, transmitted_by tick bites and transmitted_by contact with infected person. The infection has_symptom fever, has_symptom headache, has_symptom cough, has_symptom pleuritic chest pain, has_symptom myalgia and has_symptom arthralgia. [-]
qualitative platelet defect	Qualitative platelet deficiency; Qualitative plate.. [+] Qualitative platelet deficiency; Qualitative platelet deficiency NOS (disorder) [-]	n_a
quadriplegia	tetraplegia	n_a
quinidine allergy	Kinidin allergy	A drug allergy that has_allergic_trigger quinidine..[+] A drug allergy that has_allergic_trigger quinidine. [-]
Qazi Markouizos syndrome	Qazi-Markouizos syndrome; Dysharmonic skeletal mat.. [+] Qazi-Markouizos syndrome; Dysharmonic skeletal maturation - muscular fibre disproportion [-]	A syndrome that is characterized by hypotonia, con..[+] A syndrome that is characterized by hypotonia, congenital fiber type disproportion and dysharmonic skeletal maturation. [-]
Quebec platelet disorder	BDPLT5; platelet-type bleeding disorder 5; factor .. [+] BDPLT5; platelet-type bleeding disorder 5; factor V Quebec [-]	A blood platelet disease characterized by autosoma..[+] A blood platelet disease characterized by autosomal dominant inheritance of delayed onset bleeding after challenge, moderate to severe bleeding tendencies, frequent ecchymoses, mucocutaneous bleeding, muscle and joint bleeds and platelet alpha-granule degredation that has_material_basis_in heterozygous tandem duplication of the PLAU gene on chromosome 10q22. [-]
angioedema	Quincke's edema; angioneurotic edema; giant urtica.. [+] Quincke's edema; angioneurotic edema; giant urticaria; Angioneurotic oedema [-]	A skin disease characterized by one or more areas ..[+] A skin disease characterized by one or more areas of well-demarcated, non-pitting edema of deep subcutaneous tissues. [-]
chronic granulomatous disease	Quie syndrome; Bridges-Good syndrome; Congenital d.. [+] Quie syndrome; Bridges-Good syndrome; Congenital dysphagocytosis; CGD [-]	A phagocyte bactericidal dysfunction characterized..[+] A phagocyte bactericidal dysfunction characterized by an inability to resist repeated infectious diseases and a tendency to develop chronic inflammation. Life-threatening recurrent fungal and bacterial infections affecting the skin, lungs, and bones may occur along with swollen areas of inflamed tissues known as granulomas that can be widely distributed. [-]
penis carcinoma in situ	Queyrat's erythroplasia; carcinoma in situ of peni.. [+] Queyrat's erythroplasia; carcinoma in situ of penis; Penile intraepithelial neoplasia grade III; grade III squamous Intraepithelial Lesion of penis; Bowen's disease of penis [-]	An in situ carcinoma that is located_in the penis.
spastic quadriplegic cerebral palsy	quadriplegic infantile cerebral palsy; spastic qua.. [+] quadriplegic infantile cerebral palsy; spastic quadriplegic cerebral palsy; tetraplegic infantile cerebral palsy; inherited congenital spastic quadriplegia; inherited congenital spastic tetraplegia; spastic quadriplegia [-]	A spastic cerebral palsy that is characterized by ..[+] A spastic cerebral palsy that is characterized by non-progressive, variable spastic quadriparesis in multiple members of a family, in the absence of additional factors complicating pregnancy or birth, affecting all four limbs, and with difficulty with walking and talking. [-]
trench fever	Quintan fever; His-Werner disease; Trench fever; t.. [+] Quintan fever; His-Werner disease; Trench fever; tibialgic fever; shin bone fever; Wolhynian fever [-]	A primary bacterial infectious disease that result..[+] A primary bacterial infectious disease that results in systemic infection, has_material_basis_in Bartonella quintana, which is transmitted by body lice (Pediculus humanus corporis). The infection has symptom relapsing fever, has symptom headache, has symptom shin pain, and has symptom soreness of the muscles of the legs and back. [-]
Plasmodium malariae malaria	Quartan Malaria; Malaria by Plasmodium malariae	A malaria caused by a parasite Plasmodium malariae..[+] A malaria caused by a parasite Plasmodium malariae, which is marked by recurrence of paroxysms at 72-hour intervals. [-]
C1 inhibitor deficiency	Quincke edema	A complement deficiency that is a functional defic..[+] A complement deficiency that is a functional deficiency in the complement component C1 inhibitor leading to hereditary angioedema (HAE) involving swelling due to leakage of fluid from blood vessels into connective tissue. [-]
combined oxidative phosphorylation deficiency 40	QRSL1-related COXPD; COXPD40	A combined oxidative phosphorylation deficiency th..[+] A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in QRSL1 on chromosome 6q21. [-]

Page(s): 1