luliyucoordinate / json-parser Goto Github PK

$ python json.v1.py

json.decoder.JSONDecodeError: Invalid control character at: line 17 column 186 (char 987)

{
    "omim": {
        "version": "1.0",
        "entryList": [
            {
                "entry": {
                    "prefix": "#",
                    "mimNumber": 618541,
                    "status": "live",
                    "titles": {
                        "preferredTitle": "HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT; HOD"
                    },
                    "clinicalSynopsis": {
                        "inheritance": "Autosomal dominant {SNOMEDCT:263681008} {UMLS C0443147 HP:0000006} {HPO HP:0000006 C0443147}",
                        "growthHeight": "Short stature {SNOMEDCT:422065006,237837007,237836003} {ICD10CM:R62.52,E34.3} {ICD9CM:783.43} {UMLS C0013336,C0349588,C2237041,C2919142 HP:0004322,HP:0003510} {HPO HP:0004322 C0349588}",
                        "growthOther": "Intrauterine growth retardation {SNOMEDCT:22033007} {ICD9CM:764.90,764.9} {UMLS C0015934 HP:0001511} {HPO HP:0001511 C0015934,C0021296,C1386048};\nPostnatal delayed growth",
                        "headAndNeckEars": "Profound hearing loss, unilateral (patient 1)",
                        "headAndNeckEyes": "Normally pigmented irides;\nReduced visual acuity (patient 1) {HPO HP:0007663 C0234632};\nRod-cone dystrophy seen on electroretinography (patient 1)",
                        "abdomenLiver": "Hepatomegaly {SNOMEDCT:80515008} {ICD10CM:R16.0} {ICD9CM:789.1} {UMLS C0019209 HP:0002240} {HPO HP:0002240 C0019209};\nAbnormal cytoplasmic inclusion bodies in hepatic macrophages",
                        "abdomenSpleen": "Splenomegaly {SNOMEDCT:16294009} {ICD10CM:R16.1} {ICD9CM:789.2} {UMLS C0038002 HP:0001744} {HPO HP:0001744 C0038002}",
                        "abdomenGastrointestinal": "Abnormal cytoplasmic inclusion bodies in duodenal histiocytes",
                        "genitourinaryKidneys": "Enlarged kidneys {SNOMEDCT:300444006} {UMLS C0542518 HP:0000105};\nPoor corticomedullary differentiation;\nAbnormal cytoplasmic inclusion bodies in renal interstitial macrophages",
                        "skeletalLimbs": "Short long bones {UMLS C1854912 HP:0003026};\nDiffuse hypermobility of upper extremities (patient 1)",
                        "skinNailsHairSkin": "Hypopigmentation {SNOMEDCT:18655006,23006000,89031001} {UMLS C1963139,C0162835 HP:0001010} {HPO HP:0001010 C0162835}",
                        "skinNailsHairSkinElectronMicroscopy": "Abnormal cytoplasmic inclusion bodies in interstitial macrophages;\nImmature melanosomes;\nDisorganized melanosomes",
                        "skinNailsHairHair": "Hypopigmentation {SNOMEDCT:18655006,23006000,89031001} {UMLS C1963139,C0162835 HP:0001010} {HPO HP:0001010 C0162835}",
                        "muscleSoftTissue": "Decreased muscle mass in lower extremities (patient 1)",
                        "neurologicCentralNervousSystem": "Delayed gross motor development {SNOMEDCT:430099007} {UMLS C1837658 HP:0002194} {HPO HP:0002194 C1837658};\nDelayed fine motor development {UMLS C4023681 HP:0010862} {HPO HP:0010862 C4023681};\nGeneralized hypotonia (patient 1) {HPO HP:0001290 C1858120};\nSustained clonus of lower extremities (patient 2);\nMyoclonic jerks of lower extremities (patient 2);\nDelayed myelination seen on brain MRI;\nHyperintensity of subthalamic nuclei;\nThin posterior corpus callosum {UMLS C4228794};\nCerebellar atrophy {UMLS C0740279 HP:0001272} {HPO HP:0001272 C0262404,C0740279,C4020873}",
                        "prenatalManifestationsAmnioticFluid": "Polyhydramnios {SNOMEDCT:86203003} {ICD10CM:O40} {ICD9CM:657,657.0} {UMLS C0020224 HP:0001561} {HPO HP:0001561 C0020224}",
                        "prenatalManifestationsDelivery": "Premature birth {SNOMEDCT:282020008,49550006,367494004} {ICD9CM:644.2} {UMLS C0233315,C0151526,C2028283 HP:0001622} {HPO HP:0001622 C0151526,C0233315}",
                        "laboratoryAbnormalities": "Enlarged lysosomal storage vacuoles in liver, spleen, and kidney",                        "miscellaneous": "Based on report of 2 unrelated children, ages 22 months and 14 months (last curated August 2019)",
                        "molecularBasis": "Caused by mutation in the chloride channel-7 gene (CLCN7, {602727.0007})"
                    }
                }
            }
        ]
    }
}