[
    "You are an expert in the field of rare disease. You will be provided and asked about a complicated clinical case; read it carefully and then provide a diverse and comprehensive differential diagnosis.Patient's phenotype: Cholecystitis,Cerebral hemorrhage,Ascites,Abnormal mitral valve morphology,Cardiomegaly,Pericardial effusion,Abnormal tricuspid valve morphology,Right ventricular failure,Accessory spleen,Abdominal pain,Pulmonary arterial hypertension,Dyspnea,Pleural effusion,Sparse scalp hair,Hepatomegaly,Conjugated hyperbilirubinemia,Generalized muscle weakness,Exercise intolerance,Increased total bilirubin,Permanent atrial fibrillation,Pulmonary artery dilatation,Abnormal vena cava morphology,Reduced systolic function,Pedal edema,Decreased urine output,Reduced left ventricular ejection fraction,Left ventricular diastolic dysfunction,Right atrial enlargement,Increased circulating NT-proBNP concentration,Left atrial enlargement\n, The rare disease he/she suffers from is [Cardiomyopathy, familial restrictive, 1,家族性/特发性限制型心肌病/Familial/Idiopathic restrictive cardiomyopathy,Cardiomyopathy, familial restrictive, 3,Cardiomyopathy, dilated, 1KK,Cardiomyopathy, familial hypertrophic, 26]. Please write down the reasoning process, no more than 5 reasoning steps. Let's think step by step.",
    "You are an expert in the field of rare disease. You will be provided and asked about a complicated clinical case; read it carefully and then provide a diverse and comprehensive differential diagnosis.Patient's phenotype: Oral ulcer,Increased circulating renin level,Syncope,Palpitations,Diarrhea,Dyspnea,Hypokalemia,Hypomagnesemia,Generalized muscle weakness,Lower limb muscle weakness,Paroxysmal vertigo,T-wave inversion,Abnormality of urine calcium concentration,Nodular regenerative hyperplasia of liver,Dysesthesia,Amaurosis fugax\n The rare disease he/she suffers from is [Gitelman 综合征/Gitelman syndrome; GS/Gitelman syndrome/Gitelman syndrome,Gitelman 综合征/Gitelman syndrome; GS/Gitelman syndrome/Gitelman syndrome,Gitelman 综合征/Gitelman syndrome; GS/Gitelman syndrome/Gitelman syndrome]. Please write down the reasoning process, no more than 5 reasoning steps. Let's think step by step.",
    "You are an expert in the field of rare disease. You will be provided and asked about a complicated clinical case; read it carefully and then provide a diverse and comprehensive differential diagnosis.Patient's phenotype: Proteinuria,Glomerulonephritis,Hearing impairment,Visual loss,Fever,Hypercholesterolemia,Elevated circulating creatinine concentration,Elevated erythrocyte sedimentation rate,Recurrent tonsillitis,Abnormal urinary color,Macroscopic hematuria\n The rare disease he/she suffers from is [Alport syndrome, X-linked,Alport syndrome 2, autosomal recessive,Alport syndrome 3, autosomal dominant,Alport 综合征/Alport syndrome/Alport syndrome,Alport 综合征/Alport syndrome/Alport syndrome]. Please write down the reasoning process, no more than 5 reasoning steps. Let's think step by step."
]