{"uid":"cap_7pTAEgpwVQq9feqTMaZ6l","slug":"ncbi-omim-genetic-disorder-search-via-e-utilities-7d4da7c2","name":"NCBI OMIM Genetic Disorder Search via E-utilities","description":"Search the NCBI OMIM (Online Mendelian Inheritance in Man) genetic-disorder database and return matching UIDs for query {q} via E-utilities. Query: ?q= Returns JSON.","url":"https://clonecho.builda.company/x402/s/ncbi-esearch-omim","method":"POST","headers":{},"bodySchema":null,"responseSchema":null,"example":null,"exampleRequest":null,"tags":["x402"],"displayCostAmount":"0.02","displayCostAsset":"USDC","priceDynamic":false,"priceHint":null,"priceStatus":"priced","priceSource":"registry","requiresHandshake":false,"reviewCount":0,"rating":{"score":"0.00","successRate":"0.00","reviews":0,"stars":null,"state":"unrated"},"availabilityStatus":"unknown","priceObserved":null,"sessionDeposit":null,"pricing":{"kind":"static","summary":"$0.02/call","primary":{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.02","per":"call","confidence":"exact"},"accepted":[{"kind":"static","protocol":"x402","network":"base","amountUsd":"0.02","per":"call","confidence":"exact"}]},"paymentMethods":[{"uid":"pm_1WteweNSnIusz_K9Os8v-","protocol":"x402","methodType":"crypto","chain":"base","mode":"charge","costAmount":"0.02","costPer":"request","priority":0,"asset":"0x036CbD53842c5426634e7929541eC2318f3dCF7e","unit":"request","depositMicros":null,"planRef":null}],"brandName":null,"brandSlug":null,"brandBaseUrl":null,"brandDocsUrl":null,"whatItDoes":"Searches the NCBI OMIM (Online Mendelian Inheritance in Man) database using NCBI E-utilities and returns matching UIDs for a given query string.","exampleAgentPrompt":"Search the NCBI OMIM database for 'Marfan syndrome' and give me the matching OMIM UIDs.","exampleUseCases":null,"resultDescription":"A JSON object containing OMIM UIDs (numerical identifiers) that match the search query, along with metadata such as result count, query key, and WebEnv session token from NCBI E-utilities.","failureModes":["Empty result set if the query matches no OMIM records","Malformed or missing query parameter returns an error","NCBI E-utilities rate limiting may cause transient failures","Very broad queries may return a large number of UIDs without ranking","Service unavailability if upstream NCBI API is down"],"whenToPreferThis":"Use this endpoint when you need to search the authoritative OMIM database for genetic disorders, hereditary conditions, or gene-disease associations and retrieve their canonical NCBI UIDs for downstream lookups. Prefer this over general web search when you need structured, machine-readable genetic disorder identifiers from the NCBI ecosystem.","instructions":null,"reviewSummary":null,"reviewSummaryHighlights":null,"reviewSummaryConcerns":null,"reviewSummaryGeneratedAt":null,"activationCount":0,"lastUsedAt":null,"lastSuccessfullyRanAt":null,"lastHealthCheckAt":"2026-09-14T07:21:44.951Z","isFirstParty":false}