| Disease Browser
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Parent Node:
 brain disease (MONDO:0005560) |
Parent Node:
hypnic headache (disease) (MONDO:0017181) |
Parent Node:
neurovascular disease (MONDO:0043218) |
..Starting node
.. migraine disorder ()
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Child Nodes:
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| ........MGR12 () |
| ........migraine with aura () |
| ........migraine with or without aura, susceptibility to, 1 () |
| ........migraine with or without aura, susceptibility to, 10 () |
| ........migraine with or without aura, susceptibility to, 11 () |
| ........migraine with or without aura, susceptibility to, 3 () |
| ........migraine with or without aura, susceptibility to, 5 () |
| ........migraine with or without aura, susceptibility to, 8 () |
| ........migraine without aura () |
| ........migraine, familial hemiplegic, 1 () |
| ........migraine, with or without aura, susceptibility to, 13 () |
Sister Nodes: |
..ataxia - telangiectasia-like disorder ()
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..ataxia telangiectasia ()
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..Bannayan-Riley-Ruvalcaba syndrome ()
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..basal laminar drusen ()
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..benign choroid plexus neoplasm ()
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..benign neoplasm of choroid ()
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..campomelia, Cumming type ()
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..carotid body paraganglioma ()
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..cavernous sinus meningioma ()
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..central areolar choroidal dystrophy ()
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..central nervous system angiosarcoma ()
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..central nervous system hemangioma ()
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..central nervous system vasculitis ()
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..cerebral sinovenous thrombosis ()
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..cerebral visual impairment ()
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..cerebrovascular disorder ()
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..Char syndrome ()
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..choroid cancer ()
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..choroid plexus cancer ()
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..choroidal sclerosis ()
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..choroideremia ()
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..Cryoglobulinemic vasculitis ()
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..deafness-lymphedema-leukemia syndrome ()
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..eosinophilic granulomatosis with polyangiitis ()
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..erythromelalgia ()
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..eyelid capillary hemangioma ()
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..Fabry disease ()
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..genetic central nervous system and retinal vascular disease ()
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..gyrate atrophy ()
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..hemangioblastoma ()
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..hemangioma of retina ()
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..Hennekam syndrome ()
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..hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency ()
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..intracranial hypertension ()
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..jugulotympanic paraganglioma ()
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..macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome ()
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..median arcuate ligament syndrome ()
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..Meige disease ()
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..microcephaly with or without chorioretinopathy, lymphedema, or mental retardation ()
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..microcephaly-capillary malformation syndrome ()
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..microscopic polyangiitis ()
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..migraine disorder ()
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..neoplasm of aortic body ()
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..neurofibromatosis type 1 ()
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..Norman-Roberts syndrome ()
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..paragangliomas 1 ()
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..paragangliomas 2 ()
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..paragangliomas 3 ()
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..paragangliomas 4 ()
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..paragangliomas 5 ()
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..PEHO syndrome ()
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..pelvis syndrome ()
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..polyarteritis nodosa ()
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..prolidase deficiency ()
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..Proteus syndrome ()
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..retinal dystrophies primarily involving Bruch's membrane ()
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..retinal ischemia ()
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..retinal vascular disease ()
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..simple cryoglobulinemia ()
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..sporadic pheochromocytoma/secreting paraganglioma ()
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..Sturge-Weber syndrome ()
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..subarachnoid hemorrhage (disease) ()
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..trigeminal autonomic cephalalgia ()
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..Williams syndrome ()
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..Wyburn-Mason syndrome ()
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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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