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congenital secretory sodium diarrhea 3 | idiopathic generalized epilepsy 8 | 0 |
congenital secretory sodium diarrhea 3 | charcot-marie-tooth disease type 1 | 0 |
congenital secretory sodium diarrhea 3 | speech disorder | 0 |
congenital secretory sodium diarrhea 3 | congenital disorder of glycosylation ig | 0 |
congenital secretory sodium diarrhea 3 | gliosarcoma | 0 |
congenital secretory sodium diarrhea 3 | stormorken syndrome | 0 |
congenital secretory sodium diarrhea 3 | charcot-marie-tooth disease axonal type 2x | 0 |
congenital secretory sodium diarrhea 3 | giant cell glioblastoma | 0 |
hemoglobin c disease | hemoglobinopathy | 1 |
hemoglobin c disease | hemoglobin d disease | 0 |
hemoglobin c disease | methemoglobinemia | 0 |
hemoglobin c disease | hemoglobin e disease | 0 |
hemoglobin c disease | schwannoma of twelfth cranial nerve | 0 |
hemoglobin c disease | sotos syndrome 2 | 0 |
hemoglobin c disease | myopia | 0 |
hemoglobin c disease | semantic agnosia | 0 |
hemoglobin c disease | coenurosis | 0 |
hemoglobin c disease | sabinas brittle hair syndrome | 0 |
hemoglobin c disease | nominal aphasia | 0 |
carotid stenosis | carotid artery disease | 1 |
carotid stenosis | carotid artery thrombosis | 0 |
carotid stenosis | carotid artery dissection | 0 |
carotid stenosis | mixed hepatoblastoma | 0 |
carotid stenosis | familial isolated trichomegaly | 0 |
carotid stenosis | acute biphenotypic leukemia | 0 |
carotid stenosis | breast fibroadenosis | 0 |
carotid stenosis | primary ciliary dyskinesia 35 | 0 |
carotid stenosis | bladder squamous cell carcinoma | 0 |
carotid stenosis | epidural spinal canal neoplasm | 0 |
carotid stenosis | congenital epulis | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | catecholaminergic polymorphic ventricular tachycardia | 1 |
catecholaminergic polymorphic ventricular tachycardia 4 | catecholaminergic polymorphic ventricular tachycardia 2 | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | catecholaminergic polymorphic ventricular tachycardia 3 | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | catecholaminergic polymorphic ventricular tachycardia 1 | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | catecholaminergic polymorphic ventricular tachycardia 5 | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | autosomal recessive nonsyndromic deafness 25 | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | meniere's disease | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | menkes disease | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | saldino-noonan syndrome | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | boutonneuse fever | 0 |
catecholaminergic polymorphic ventricular tachycardia 4 | autosomal recessive intellectual developmental disorder 60 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy | 1 |
myofibrillar myopathy 8 | myofibrillar myopathy 3 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 9 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 5 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 4 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 1 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 6 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 2 | 0 |
myofibrillar myopathy 8 | fatal infantile hypertonic myofibrillar myopathy | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 10 | 0 |
myofibrillar myopathy 8 | myofibrillar myopathy 7 | 0 |
familial hemiplegic migraine 3 | familial hemiplegic migraine | 1 |
familial hemiplegic migraine 3 | familial hemiplegic migraine 1 | 0 |
familial hemiplegic migraine 3 | familial hemiplegic migraine 2 | 0 |
familial hemiplegic migraine 3 | timothy grass allergy | 0 |
familial hemiplegic migraine 3 | distal hereditary motor neuronopathy type 2a | 0 |
familial hemiplegic migraine 3 | charcot-marie-tooth disease type 2dd | 0 |
familial hemiplegic migraine 3 | desmoplastic infantile ganglioglioma | 0 |
familial hemiplegic migraine 3 | angiomyolipoma | 0 |
familial hemiplegic migraine 3 | silo filler's disease | 0 |
familial hemiplegic migraine 3 | macrotrabecular hepatoblastoma | 0 |
familial hemiplegic migraine 3 | eyelid benign neoplasm | 0 |
constrictive pericarditis | pericarditis | 1 |
constrictive pericarditis | chronic rheumatic pericarditis | 0 |
constrictive pericarditis | histoplasmosis pericarditis | 0 |
constrictive pericarditis | dressler's syndrome | 0 |
constrictive pericarditis | heart conduction disease | 0 |
constrictive pericarditis | acute eustachian salpingitis | 0 |
constrictive pericarditis | pseudobulbar palsy | 0 |
constrictive pericarditis | cleidocranial dysplasia | 0 |
constrictive pericarditis | vitamin d-dependent rickets type 1a | 0 |
constrictive pericarditis | salivary gland adenoid cystic carcinoma | 0 |
constrictive pericarditis | platelet-type bleeding disorder 18 | 0 |
pericardium leiomyoma | cardiovascular organ benign neoplasm | 1 |
pericardium leiomyoma | benign perivascular tumor | 0 |
pericardium leiomyoma | cerebrovascular benign neoplasm | 0 |
pericardium leiomyoma | heart lipoma | 0 |
pericardium leiomyoma | cardiac granular cell neoplasm | 0 |
pericardium leiomyoma | hemangioma | 0 |
pericardium leiomyoma | venous hemangioma | 0 |
pericardium leiomyoma | benign pericardial teratoma | 0 |
pericardium leiomyoma | benign vascular tumor | 0 |
pericardium leiomyoma | osteopathia striata with cranial sclerosis | 0 |
pericardium leiomyoma | nuclear type mitochondrial complex i deficiency 21 | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy | 1 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 8 | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 9 | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 10 | 0 |
progressive myoclonus epilepsy 4 | unverricht-lundborg syndrome | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 3 | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 7 | 0 |
progressive myoclonus epilepsy 4 | progressive myoclonus epilepsy 6 | 0 |
progressive myoclonus epilepsy 4 | lafora disease | 0 |
progressive myoclonus epilepsy 4 | residual stage corticosteroid-induced glaucoma | 0 |
progressive myoclonus epilepsy 4 | autosomal recessive limb-girdle muscular dystrophy type 2h | 0 |
acute gonococcal cystitis | acute cystitis | 1 |
acute gonococcal cystitis | nuclear type mitochondrial complex i deficiency 7 | 0 |
acute gonococcal cystitis | alzheimer's disease 5 | 0 |
acute gonococcal cystitis | 46,xy sex reversal 1 | 0 |