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Disease	Synonyms	Description	Articles
jejunal cancer	malignant neoplasm of jejunum; malignant tumor of .. [+] malignant neoplasm of jejunum; malignant tumor of jejunum (disorder); malignant tumor of jejunum [-]	n_a
Johanson-Blizzard syndrome	JBS; Johanson-Blizzard syndrome (disorder)	A syndrome that involves abnormal development of t..[+] A syndrome that involves abnormal development of the pancreas, nose and scalp, with mental retardation, hearing loss and growth failure. It is inherited in an autosomal recessive manner. [-]
juvenile ankylosing spondylitis		An autoimmune disease of musculoskeletal system th..[+] An autoimmune disease of musculoskeletal system that is an ankylosing spondylitis with onset during childhood. [-]
Japanese spotted fever	oriental spotted fever; Rickettsia japonica spotte.. [+] oriental spotted fever; Rickettsia japonica spotted fever [-]	A spotted fever that has_material_basis_in Rickett..[+] A spotted fever that has_material_basis_in Rickettsia japonica, which is transmitted_by ticks (Dermacentor taiwanensis and Haemaphysalis flava). The infection has_symptom fever, has_symptom eschars, has_symptom regional adenopathy, and has_symptom rash on extremities. [-]
juvenile myelomonocytic leukemia		A myelodysplastic/myeloproliferative neoplasm that..[+] A myelodysplastic/myeloproliferative neoplasm that is characterized by the uncontrolled growth of monocytes. [-]	1 articles
Joubert syndrome	JBTS	A ciliopathy that is characterized by congenital m..[+] A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. [-]	5 articles
juvenile polyposis syndrome		A gastrointestinal system disease that is characte..[+] A gastrointestinal system disease that is characterized by predisposition to hamartomatous benign polyps in the gastrointestinal tract, specifically in the stomach, small intestine, colon, and rectum. [-]
jejunal adenocarcinoma		A jejunal cancer that is located_in the jejunum an..[+] A jejunal cancer that is located_in the jejunum and has_material_basis_in epithelial tissue that has glandular origin. [-]
janus kinase-3 deficiency		n_a
juvenile absence epilepsy		An adolescence-adult electroclinical syndrome stat..[+] An adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures. [-]
jejunoileitis		An inflammatory bowel disease that is characterize..[+] An inflammatory bowel disease that is characterized by patchy areas of inflammation located_in jejunum, has_symptom abdominal pain, has_symptom diarrhea, has_symptom cramps and has_symptom formation of fistulas. [-]
Joubert syndrome with orofaciodigital defect	OFD6; Varadi-Papp syndrome; Polydactyly cleft lip .. [+] OFD6; Varadi-Papp syndrome; Polydactyly cleft lip palate psychomotor retardation; Varadi syndrome; orofaciodigital syndrome VI [-]	A Joubert syndrome that is characterized by orofac..[+] A Joubert syndrome that is characterized by orofaciodigital defect. [-]
junctional epidermolysis bullosa with pyloric atresia	junctional epidermolysis bullosa-pyloric atresia s.. [+] junctional epidermolysis bullosa-pyloric atresia syndrome; JEB-PA; Carmi syndrome; epidermolysis bullosa junctionalis with pyloric atresia [-]	A junctional epidermolysis bullosa characterized b..[+] A junctional epidermolysis bullosa characterized by generalized blistering at birth with congenital atresia of the pylorus and rarely of other portions of the gastrointestinal tract and that has_material_basis_in mutations in the ITGB4 or ITGA6 genes. [-]
junctional epidermolysis bullosa Herlitz type	JEB-Herlitz type; junctional epidermolysis bullosa.. [+] JEB-Herlitz type; junctional epidermolysis bullosa, Herlitz-Pearson type; junctional epidermolysis bullosa generalisata gravis; JEB-H; Herlitz type epidermolysis bullosa junctionalis; Herlitz-Pearson-type epidermolysis bullosa; epidermolysis bullosa letalis [-]	A junctional epidermolysis bullosa characterized b..[+] A junctional epidermolysis bullosa characterized by autosomal recessive inheritance of severe blisters and extensive erosions, localized to the skin and mucous membranes, resulting in a failure to thrive and that has_material_basis_in mutations in any 1 of the 3 genes encoding the subunits of laminin-5: LAMA3, LAMB3, and LAMC2. The Herlitz type is more severe than the related non-Herlitz type of junctional epidermolysis bullosa. [-]
junctional epidermolysis bullosa non-Herlitz type	junctional epidermolysis bullosa, Disentis type; j.. [+] junctional epidermolysis bullosa, Disentis type; junctional epidermolysis bullosa generalisata mitis; JEN-nH; JEB-nH gen; GABEB; generalized atrophic benign epidermolysis bullosa; generalized junctional epidermolysis bullosa, non-Herlitz type [-]	A junctional epidermolysis bullosa characterized b..[+] A junctional epidermolysis bullosa characterized by skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in several genes including COL17A1, ITGB4 and the 3 genes that encode the subunits of laminin-5: LAMA3, LAMB3, and LAMC2. The non-Herlitz type is less severe than the related Herlitz type of junctional epidermolysis bullosa. [-]
juvenile-onset Parkinson disease		n_a
Jansen's metaphyseal chondrodysplasia	Jansen metaphyseal chondrodysplasia; Jansen Metaph.. [+] Jansen metaphyseal chondrodysplasia; Jansen Metaphyseal Dysostosis; Jansen Disease; Murk Jansen Type Metaphyseal Chondrodysplasia [-]	A metaphyseal dysplasia that has_material_basis_in..[+] A metaphyseal dysplasia that has_material_basis_in mutation in PTH receptor which results_in short-limbed dwarfism. [-]
Joubert syndrome 30		A Joubert syndrome that has_material_basis_in homo..[+] A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ARMC9 gene on chromosome 2q37. [-]
Joubert syndrome 31		A Joubert syndrome that has_material_basis_in homo..[+] A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP120 gene on chromosome 5q23. [-]
Joubert syndrome 33		A Joubert syndrome that has_material_basis_in homo..[+] A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the PIBF1 gene on chromosome 13q21. [-]

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