| Disease Browser
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Parent Node:
 nervous system disorder (MONDO:0005071) |
..Starting node
.. genetic nervous system disorder ()
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Child Nodes:
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| ........Aase-Smith syndrome () |
| ........acrofacial dysostosis Rodriguez type () |
| ........acrofacial dysostosis, Catania type () |
| ........alopecia - contractures - dwarfism - intellectual disability syndrome () |
| ........alopecia - intellectual disability syndrome () |
| ........alopecia-epilepsy-pyorrhea-intellectual disability syndrome () |
| ........alpha thalassemia-intellectual disability syndrome type 1 () |
| ........aniridia-cerebellar ataxia-intellectual disability syndrome () |
| ........aniridia-renal agenesis-psychomotor retardation syndrome () |
| ........ataxia-pancytopenia syndrome () |
| ........Bannayan-Riley-Ruvalcaba syndrome () |
| ........benign paroxysmal positional nystagmus () |
| ........blepharonasofacial malformation syndrome () |
| ........c syndrome () |
| ........cardiocranial syndrome, Pfeiffer type () |
| ........cataract-hypertrichosis-intellectual disability syndrome () |
| ........cataract-intellectual disability-hypogonadism syndrome () |
| ........cerebrofaciothoracic dysplasia () |
| ........Chiari malformation type I () |
| ........Chiari malformation type II () |
| ........cluster headache, familial () |
| ........coloboma of optic nerve (disease) () |
| ........corpus callosum, agenesis of () |
| ........craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome () |
| ........craniotelencephalic dysplasia () |
| ........Czeizel-Losonci syndrome () |
| ........Dandy-Walker malformation-postaxial polydactyly syndrome () |
| ........Dandy-Walker syndrome () |
| ........Dubowitz syndrome () |
| ........encephalopathy, recurrent, of childhood () |
| ........endosteal sclerosis-cerebellar hypoplasia syndrome () |
| ........familial congenital palsy of trochlear nerve () |
| ........familial hemiplegic migraine () |
| ........Flynn-Aird syndrome () |
| ........fowler syndrome () |
| ........Frey syndrome () |
| ........gapo syndrome () |
| ........GLUT1 deficiency syndrome () |
| ........GMS syndrome () |
| ........hepatic fibrosis-renal cysts-intellectual disability syndrome () |
| ........hereditary night blindness () |
| ........hydrolethalus syndrome () |
| ........Johnson neuroectodermal syndrome () |
| ........linear nevus sebaceus syndrome () |
| ........major affective disorder 1 () |
| ........melanoma and neural system tumor syndrome () |
| ........Meniere disease () |
| ........Muir-Torre syndrome () |
| ........nevoid basal cell carcinoma syndrome () |
| ........nystagmus, hereditary vertical () |
| ........obsessive-compulsive disorder () |
| ........orofaciodigital syndrome V () |
| ........orofaciodigital syndrome X () |
| ........panic disorder 1 () |
| ........paragangliomas 1 () |
| ........paragangliomas 4 () |
| ........paroxysmal extreme pain disorder () |
| ........primary basilar invagination () |
| ........Proteus syndrome () |
| ........pseudopapilledema (disease) () |
| ........retinal detachment () |
| ........Shprintzen-Goldberg syndrome () |
| ........Smith-Magenis syndrome () |
| ........stuttering, familial persistent, 1 () |
| ........trichorhinophalangeal syndrome type II () |
| ........ventriculomegaly-cystic kidney disease () |
Sister Nodes: |
..autoimmune disease of the nervous system ()
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..Balint syndrome ()
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..Barre-Lieou syndrome ()
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..central nervous system disease ()
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..cerebral disease with cataract ()
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..complex neurodevelopmental disorder ()
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..congenital nervous system disorder ()
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..cranial nerve neuropathy ()
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..developmental disability ()
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..diplegia of upper limb ()
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..drug-induced akathisia ()
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..drug-induced dyskinesia ()
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..genetic nervous system disorder ()
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..Gerstmann syndrome ()
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..idiopathic recurrent stupor ()
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..infectious disease of the nervous system ()
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..inherited nervous system cancer-predisposing syndrome ()
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..locked-in syndrome ()
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..movement disorder ()
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..neonatal brainstem dysfunction ()
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..nervous system injury ()
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..nervous system neoplasm ()
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..neurocutaneous syndrome ()
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..neuroendocrine disease ()
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..neuronitis ()
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..neurosarcoidosis ()
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..neurovascular disease ()
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..palsy ()
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..paraneoplastic neurologic syndrome ()
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..perceptual disorders ()
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..perineural cyst ()
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..peripheral nervous system disease ()
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..persistent idiopathic facial pain ()
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..primary orthostatic hypotension ()
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..radiculitis ()
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..rare disease with malignant hyperthermia ()
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..rare neuroinflammatory or neuroimmunological disease ()
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..rare neurologic disease with psychiatric involvement ()
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..restless legs syndrome ()
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..retinal disease ()
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..sensory ganglionopathy ()
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..sleep-wake disorder ()
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..specific learning disability ()
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..spontaneous periodic hypothermia ()
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..symmetrical thalamic calcifications ()
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..toxic encephalopathy ()
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..Wallerian degeneration ()
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..Worster-Drought 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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