79 lines
2.0 KiB
Plaintext
79 lines
2.0 KiB
Plaintext
inou Health API
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===============
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Base URL: https://inou.com
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Authentication: Bearer token in Authorization header, or token query parameter.
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Your token is your dossier ID (16-character hex).
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Example: Authorization: Bearer abc123def456789a
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DATA TYPES
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----------
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- Imaging: MRI, CT, X-ray, ultrasound (DICOM format)
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- Labs: Blood tests, metabolic panels, etc.
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- Genome: SNP variants with clinical annotations
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IMAGING ENDPOINTS
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-----------------
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GET /api/v1/dossiers
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List all dossiers accessible to your account.
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GET /api/v1/dossiers/{dossier}/entries?category=imaging
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List imaging studies for a dossier.
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GET /api/v1/dossiers/{dossier}/entries?parent={study}
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List series in a study.
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Optional: filter (e.g. T1, FLAIR, AX, SAG)
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GET /api/v1/dossiers/{dossier}/entries?parent={series}
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List slices in a series with position data.
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GET /image/{slice}?token={dossier}
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Fetch slice as PNG image.
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Optional: ww (window width), wc (window center)
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GET /contact-sheet.webp/{series}?token={dossier}
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Fetch thumbnail grid for navigation.
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Optional: ww, wc
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LAB ENDPOINTS
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-------------
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GET /api/labs/tests?dossier={dossier}
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List all available lab test names.
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GET /api/labs/results?dossier={dossier}&names={names}
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Get lab results for specified tests.
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Required: names (comma-separated test names)
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Optional: from, to (YYYY-MM-DD), latest (true/false)
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GENOME ENDPOINTS
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----------------
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GET /api/categories?dossier={dossier}
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Get top-level observation categories.
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Optional: type=genome (for genome categories)
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Optional: category={category} (for subcategories)
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GET /api/genome?dossier={dossier}
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Query genome variants.
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Optional: gene (e.g. MTHFR, COMT)
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Optional: search (gene, subcategory, or summary text)
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Optional: category (filter by category)
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Optional: rsids (comma-separated rs numbers)
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Optional: min_magnitude (0-4)
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Optional: include_hidden (true/false)
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NAVIGATION FLOW
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---------------
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Imaging: dossiers → studies → series → slices → image
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Labs: dossiers → tests → results
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Genome: dossiers → categories → variants
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