MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: central nervous system disease (MONDO:0002602)
..Starting node ..headache disorder ()
Child Nodes:
........burning mouth syndrome ()
........exertional headache ()
........hypnic headache (disease) ()
........reversible cerebral vasoconstriction syndrome ()
........spontaneous intracranial hypotension ()
Sister Nodes:
..autoimmune disease of central nervous system ()
..brain disease ()
..central nervous system infectious disorder ()
..central nervous system neoplasm ()
..central nervous system vasculitis ()
..central retinal vein occlusion ()
..cerebrospinal fluid leak ()
..encephalomyelitis ()
..headache disorder ()
..hemiplegia ()
..high pressure neurological syndrome ()
..neurodegenerative disease ()
..optic nerve disease ()
..quadriplegia ()
..spinal cord disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21146
Name:	headache disorder
Definition:	Various conditions with the symptom of headache. Headache disorders are classified into major groups, such as primary headache disorders (based on characteristics of their headache symptoms) and secondary headache disorders (based on their etiologies). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cephalgia syndrome; cephalgia syndromes; chronic daily headache; chronic daily headaches; chronic headache; chronic headaches; daily headache, chronic; daily headaches, chronic; headache disorder; headache syndrome; headache syndromes; headache, chronic; headache, chronic daily; headache, intractabl
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal