Versions

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{
    "count": 1,
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    "results": [
        {
            "id": 162,
            "hash_id": "568f860222c1fc1c79ca1769",
            "name": "Severe microcephaly",
            "disease_group": "Dysmorphic and congenital abnormality syndromes",
            "disease_sub_group": "DNA repair disorders",
            "status": "public",
            "version": "5.7",
            "version_created": "2024-05-02T13:20:12.398046Z",
            "relevant_disorders": [
                "Primary Microcephaly - Microcephalic Dwarfism Spectrum",
                "Severe microcephaly",
                "R88"
            ],
            "stats": {
                "number_of_genes": 264,
                "number_of_strs": 0,
                "number_of_regions": 7
            },
            "types": [
                {
                    "name": "Rare Disease 100K",
                    "slug": "rare-disease-100k",
                    "description": "Rare Disease 100K"
                },
                {
                    "name": "GMS Rare Disease Virtual",
                    "slug": "gms-rare-disease-virtual",
                    "description": "This is a panel for the Genomic Medicine Service for an exome/genome/panel based test that requires a virtual gene panel for rare disease in the Test Directory."
                },
                {
                    "name": "GMS signed-off",
                    "slug": "gms-signed-off",
                    "description": "This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."
                }
            ]
        }
    ]
}