Frontend Disorder Request
:param request:
:param disorder_id: primary key of disorder
:returns a JSON or HTML serialization for a disorder
:raises HTTP404 if no disorder found
GET /api/v2/disorder/1894?format=api
{
"name": "CRELD1-related Atrioventricular septal defect",
"name_alt1": null,
"name_alt2": null,
"abbr": "AVSD2",
"gene_sym": "CRELD1",
"chr_local": "3p25.3",
"aff_prot": "Cysteine-rich protein with EGF-like domains 1",
"omim_no": "606217",
"subtype": null,
"hgnc_gene_sym": "CRELD1",
"hgnc_gene_name": "",
"ncbi_gene": null,
"uniprot": null,
"kegg": null,
"treatability": "yes",
"gene_reviews": null,
"prevalence": null,
"orphacode": null,
"nosology_iem_code": "IEM1784",
"icimd_nosology_subgroup_code": "Disorders of ECM glycoproteins",
"icimd_nosology_disorder_num": "26.01.09.01",
"inheritance": "Autosomal Dominant",
"wiki_pathways": [],
"symptom_specs": {
"clinical": {
"Mitral valve cleft": {
"neonatal": "±",
"infancy": "±",
"childhood": "±",
"adolescence": "±",
"adulthood": "±",
"was_char": false,
"symptom": {
"name": "Mitral valve cleft",
"lab_name": "Mitral valve cleft",
"systems": [
"Cardiovascular"
],
"biochemical_test": null,
"hmdb": null,
"systems_ids": [
2
],
"is_lab": false
}
}
},
"clinicalchar": {
"Atrioventricular canal defect": {
"neonatal": "+",
"infancy": "+",
"childhood": "+",
"adolescence": "+",
"adulthood": "+",
"was_char": true,
"symptom": {
"name": "Atrioventricular canal defect",
"lab_name": "Atrioventricular canal defect",
"systems": [
"Cardiovascular"
],
"biochemical_test": null,
"hmdb": null,
"systems_ids": [
2
],
"is_lab": false
}
}
},
"biochemical": {}
},
"educational_documents": [],
"disorder_treatments": [],
"disorder_resources": []
}