Disease List
This API endpoint handles listing (/diseases) and retrieval (/diseases/<ID>/) of genetic diseases that are contained in the database
GET /api/diseases/?format=api
{ "data": [ { "type": "Disease", "id": "79273", "attributes": { "omim_ids": [ "OMIM121300" ], "status": "CU", "disease_name": "Hereditary coproporphyria", "icd10_category": "Endocrine, nutritional and metabolic diseases", "icd10_specificid": "E80.2", "lastmodified": "2021-10-18T11:00:45.014708" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI001" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/79273/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/79273/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/79273/?format=api" } }, { "type": "Disease", "id": "275766", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Idiopathic pulmonary arterial hypertension", "icd10_category": "Diseases of the circulatory system", "icd10_specificid": "I27.0", "lastmodified": "2021-10-18T11:00:45.017231" }, "relationships": { "combination_set": { "meta": { "count": 3 }, "data": [ { "type": "Combination", "id": "OLI002" }, { "type": "Combination", "id": "OLI003" }, { "type": "Combination", "id": "OLI004" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/275766/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/275766/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/275766/?format=api" } }, { "type": "Disease", "id": "275803", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Pulmonary arterial hypertension associated with congenital heart disease", "icd10_category": "Diseases of the circulatory system", "icd10_specificid": "I27.2", "lastmodified": "2021-10-18T11:00:45.018151" }, "relationships": { "combination_set": { "meta": { "count": 2 }, "data": [ { "type": "Combination", "id": "OLI005" }, { "type": "Combination", "id": "OLI006" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/275803/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/275803/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/275803/?format=api" } }, { "type": "Disease", "id": "2515", "attributes": { "omim_ids": [ "OMIM251220", "OMIM256370", "OMIM301028", "OMIM600995", "OMIM603278", "OMIM603965", "OMIM607832", "OMIM610725", "OMIM612551", "OMIM613237", "OMIM614131", "OMIM614196", "OMIM615244", "OMIM615573", "OMIM615861", "OMIM616002", "OMIM616032", "OMIM616220", "OMIM616730", "OMIM616892", "OMIM616893", "OMIM618176", "OMIM618177", "OMIM618178", "OMIM618179", "OMIM619201" ], "status": "CU", "disease_name": "Microcephaly-cardiomyopathy syndrome", "icd10_category": "Congenital malformations, deformations and chromosomal abnormalities", "icd10_specificid": "Q87.8", "lastmodified": "2021-10-18T11:00:45.019199" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI007" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/2515/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/2515/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/2515/?format=api" } }, { "type": "Disease", "id": "656", "attributes": { "omim_ids": [ "OMIM251220", "OMIM256370", "OMIM301028", "OMIM600995", "OMIM603278", "OMIM603965", "OMIM607832", "OMIM610725", "OMIM612551", "OMIM613237", "OMIM614131", "OMIM614196", "OMIM615244", "OMIM615573", "OMIM615861", "OMIM616002", "OMIM616032", "OMIM616220", "OMIM616730", "OMIM616892", "OMIM616893", "OMIM618176", "OMIM618177", "OMIM618178", "OMIM618179", "OMIM619201" ], "status": "CU", "disease_name": "Genetic steroid-resistant nephrotic syndrome", "icd10_category": "Diseases of the genitourinary system", "icd10_specificid": "N04", "lastmodified": "2021-10-18T11:00:45.020113" }, "relationships": { "combination_set": { "meta": { "count": 4 }, "data": [ { "type": "Combination", "id": "OLI007" }, { "type": "Combination", "id": "OLI320" }, { "type": "Combination", "id": "OLI321" }, { "type": "Combination", "id": "OLI501" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/656/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/656/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/656/?format=api" } }, { "type": "Disease", "id": "157215", "attributes": { "omim_ids": [ "OMIM241530" ], "status": "CU", "disease_name": "Hereditary hypophosphatemic rickets with hypercalciuria", "icd10_category": "Endocrine, nutritional and metabolic diseases", "icd10_specificid": "E83.3", "lastmodified": "2021-10-18T11:00:45.021045" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI008" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/157215/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/157215/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/157215/?format=api" } }, { "type": "Disease", "id": "98976", "attributes": { "omim_ids": [ "OMIM613086", "OMIM231300", "OMIM600975", "OMIM613085", "OMIM617272" ], "status": "CU", "disease_name": "Congenital glaucoma", "icd10_category": "Congenital malformations, deformations and chromosomal abnormalities", "icd10_specificid": "Q15.0", "lastmodified": "2021-10-18T11:00:45.022076" }, "relationships": { "combination_set": { "meta": { "count": 9 }, "data": [ { "type": "Combination", "id": "OLI009" }, { "type": "Combination", "id": "OLI010" }, { "type": "Combination", "id": "OLI011" }, { "type": "Combination", "id": "OLI012" }, { "type": "Combination", "id": "OLI169" }, { "type": "Combination", "id": "OLI248" }, { "type": "Combination", "id": "OLI249" }, { "type": "Combination", "id": "OLI767" }, { "type": "Combination", "id": "OLI768" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/98976/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/98976/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/98976/?format=api" } }, { "type": "Disease", "id": "87884", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Non-syndromic genetic deafness", "icd10_category": "Diseases of the ear and mastoid process", "icd10_specificid": "H90.5", "lastmodified": "2021-10-18T11:00:45.023133" }, "relationships": { "combination_set": { "meta": { "count": 15 }, "data": [ { "type": "Combination", "id": "OLI013" }, { "type": "Combination", "id": "OLI060" }, { "type": "Combination", "id": "OLI135" }, { "type": "Combination", "id": "OLI136" }, { "type": "Combination", "id": "OLI192" }, { "type": "Combination", "id": "OLI193" }, { "type": "Combination", "id": "OLI194" }, { "type": "Combination", "id": "OLI251" }, { "type": "Combination", "id": "OLI252" }, { "type": "Combination", "id": "OLI254" }, { "type": "Combination", "id": "OLI406" }, { "type": "Combination", "id": "OLI454" }, { "type": "Combination", "id": "OLI497" }, { "type": "Combination", "id": "OLI831" }, { "type": "Combination", "id": "OLI1649" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/87884/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/87884/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/87884/?format=api" } }, { "type": "Disease", "id": "95496", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Pituitary stalk interruption syndrome", "icd10_category": "Endocrine, nutritional and metabolic diseases", "icd10_specificid": "E23.6", "lastmodified": "2021-10-18T11:00:45.024301" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI014" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/95496/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/95496/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/95496/?format=api" } }, { "type": "Disease", "id": "18", "attributes": { "omim_ids": [ "OMIM179800", "OMIM267300", "OMIM602722", "OMIM611590" ], "status": "CU", "disease_name": "Distal renal tubular acidosis", "icd10_category": "Diseases of the genitourinary system", "icd10_specificid": "N25.8", "lastmodified": "2021-10-18T11:00:45.025299" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI015" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/18/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/18/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/18/?format=api" } }, { "type": "Disease", "id": "263", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Limb-girdle muscular dystrophy", "icd10_category": "Diseases of the nervous system", "icd10_specificid": "G71.0", "lastmodified": "2021-10-18T11:00:45.026220" }, "relationships": { "combination_set": { "meta": { "count": 7 }, "data": [ { "type": "Combination", "id": "OLI016" }, { "type": "Combination", "id": "OLI017" }, { "type": "Combination", "id": "OLI415" }, { "type": "Combination", "id": "OLI569" }, { "type": "Combination", "id": "OLI570" }, { "type": "Combination", "id": "OLI571" }, { "type": "Combination", "id": "OLI933" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/263/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/263/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/263/?format=api" } }, { "type": "Disease", "id": "174590", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Congenital hypogonadotropic hypogonadism", "icd10_category": "Endocrine, nutritional and metabolic diseases", "icd10_specificid": "E23.0", "lastmodified": "2021-10-18T11:00:45.027151" }, "relationships": { "combination_set": { "meta": { "count": 10 }, "data": [ { "type": "Combination", "id": "OLI018" }, { "type": "Combination", "id": "OLI019" }, { "type": "Combination", "id": "OLI020" }, { "type": "Combination", "id": "OLI650" }, { "type": "Combination", "id": "OLI651" }, { "type": "Combination", "id": "OLI652" }, { "type": "Combination", "id": "OLI653" }, { "type": "Combination", "id": "OLI654" }, { "type": "Combination", "id": "OLI1651" }, { "type": "Combination", "id": "OLI1801" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/174590/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/174590/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/174590/?format=api" } }, { "type": "Disease", "id": "388", "attributes": { "omim_ids": [ "OMIM142623", "OMIM600155", "OMIM600156", "OMIM606874", "OMIM606875", "OMIM608462", "OMIM611644", "OMIM613711", "OMIM613712" ], "status": "CU", "disease_name": "Hirschsprung disease", "icd10_category": "Congenital malformations, deformations and chromosomal abnormalities", "icd10_specificid": "Q43.1", "lastmodified": "2021-10-18T11:00:45.028119" }, "relationships": { "combination_set": { "meta": { "count": 4 }, "data": [ { "type": "Combination", "id": "OLI021" }, { "type": "Combination", "id": "OLI035" }, { "type": "Combination", "id": "OLI038" }, { "type": "Combination", "id": "OLI184" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/388/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/388/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/388/?format=api" } }, { "type": "Disease", "id": "599", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Distal myopathy", "icd10_category": "Diseases of the nervous system", "icd10_specificid": "G71.0", "lastmodified": "2021-10-18T11:00:45.029093" }, "relationships": { "combination_set": { "meta": { "count": 2 }, "data": [ { "type": "Combination", "id": "OLI022" }, { "type": "Combination", "id": "OLI1732" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/599/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/599/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/599/?format=api" } }, { "type": "Disease", "id": "1934", "attributes": { "omim_ids": [ "OMIM617493", "OMIM618548", "OMIM617599", "OMIM617391", "OMIM300672", "OMIM308350", "OMIM609304", "OMIM612164", "OMIM613402", "OMIM613721", "OMIM615473", "OMIM616341", "OMIM617276", "OMIM617389", "OMIM617350" ], "status": "CU", "disease_name": "Early infantile epileptic encephalopathy", "icd10_category": "Diseases of the nervous system", "icd10_specificid": "G40.3", "lastmodified": "2021-10-18T11:00:45.029992" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI023" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/1934/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/1934/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/1934/?format=api" } }, { "type": "Disease", "id": "144", "attributes": { "omim_ids": [ "OMIM120435", "OMIM609310", "OMIM613244", "OMIM614331", "OMIM614337", "OMIM614350", "OMIM614385" ], "status": "CU", "disease_name": "Lynch syndrome", "icd10_category": "Neoplasms", "icd10_specificid": "D48.9", "lastmodified": "2021-10-18T11:00:45.030974" }, "relationships": { "combination_set": { "meta": { "count": 2 }, "data": [ { "type": "Combination", "id": "OLI024" }, { "type": "Combination", "id": "OLI1135" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/144/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/144/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/144/?format=api" } }, { "type": "Disease", "id": "158038", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Primary hemophagocytic lymphohistiocytosis", "icd10_category": null, "icd10_specificid": null, "lastmodified": "2021-10-18T11:00:45.031955" }, "relationships": { "combination_set": { "meta": { "count": 8 }, "data": [ { "type": "Combination", "id": "OLI025" }, { "type": "Combination", "id": "OLI052" }, { "type": "Combination", "id": "OLI053" }, { "type": "Combination", "id": "OLI054" }, { "type": "Combination", "id": "OLI055" }, { "type": "Combination", "id": "OLI056" }, { "type": "Combination", "id": "OLI057" }, { "type": "Combination", "id": "OLI058" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/158038/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/158038/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/158038/?format=api" } }, { "type": "Disease", "id": "93665", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Autoinflammatory syndrome", "icd10_category": null, "icd10_specificid": null, "lastmodified": "2021-10-18T11:00:45.033030" }, "relationships": { "combination_set": { "meta": { "count": 41 }, "data": [ { "type": "Combination", "id": "OLI026" }, { "type": "Combination", "id": "OLI1750" }, { "type": "Combination", "id": "OLI1751" }, { "type": "Combination", "id": "OLI1752" }, { "type": "Combination", "id": "OLI1753" }, { "type": "Combination", "id": "OLI1754" }, { "type": "Combination", "id": "OLI1755" }, { "type": "Combination", "id": "OLI1756" }, { "type": "Combination", "id": "OLI1757" }, { "type": "Combination", "id": "OLI1758" }, { "type": "Combination", "id": "OLI1759" }, { "type": "Combination", "id": "OLI1760" }, { "type": "Combination", "id": "OLI1761" }, { "type": "Combination", "id": "OLI1762" }, { "type": "Combination", "id": "OLI1763" }, { "type": "Combination", "id": "OLI1764" }, { "type": "Combination", "id": "OLI1765" }, { "type": "Combination", "id": "OLI1766" }, { "type": "Combination", "id": "OLI1767" }, { "type": "Combination", "id": "OLI1768" }, { "type": "Combination", "id": "OLI1769" }, { "type": "Combination", "id": "OLI1770" }, { "type": "Combination", "id": "OLI1771" }, { "type": "Combination", "id": "OLI1772" }, { "type": "Combination", "id": "OLI1773" }, { "type": "Combination", "id": "OLI1774" }, { "type": "Combination", "id": "OLI1775" }, { "type": "Combination", "id": "OLI1776" }, { "type": "Combination", "id": "OLI1777" }, { "type": "Combination", "id": "OLI1778" }, { "type": "Combination", "id": "OLI1779" }, { "type": "Combination", "id": "OLI1780" }, { "type": "Combination", "id": "OLI1781" }, { "type": "Combination", "id": "OLI1782" }, { "type": "Combination", "id": "OLI1783" }, { "type": "Combination", "id": "OLI1784" }, { "type": "Combination", "id": "OLI1785" }, { "type": "Combination", "id": "OLI1786" }, { "type": "Combination", "id": "OLI1787" }, { "type": "Combination", "id": "OLI1788" }, { "type": "Combination", "id": "OLI1789" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/93665/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/93665/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/93665/?format=api" } }, { "type": "Disease", "id": "73217", "attributes": { "omim_ids": [], "status": "CU", "disease_name": "Müllerian aplasia", "icd10_category": null, "icd10_specificid": null, "lastmodified": "2021-10-18T11:00:45.033949" }, "relationships": { "combination_set": { "meta": { "count": 3 }, "data": [ { "type": "Combination", "id": "OLI027" }, { "type": "Combination", "id": "OLI028" }, { "type": "Combination", "id": "OLI029" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/73217/relationships/combination_set?format=api", "related": "https://olida.ibsquare.be/api/diseases/73217/combinations/?format=api" } } }, "links": { "self": "https://olida.ibsquare.be/api/diseases/73217/?format=api" } }, { "type": "Disease", "id": "335", "attributes": { "omim_ids": [ "OMIM202400", "OMIM616004" ], "status": "CU", "disease_name": "Congenital fibrinogen deficiency", "icd10_category": "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism", "icd10_specificid": "D68.2", "lastmodified": "2021-10-18T11:00:45.035020" }, "relationships": { "combination_set": { "meta": { "count": 1 }, "data": [ { "type": "Combination", "id": "OLI030" } ], "links": { "self": "https://olida.ibsquare.be/api/diseases/335/relationships/combination_set?format=api", "related": 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