Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandLeigh Disease (D007888)
Parent Node:
expandOptic Atrophies, Hereditary (D015418)
..Starting node
..expandNecrotizing Encephalomyelopathy, Subacute, of Leigh, Adult (C563530)

       Child Nodes:



 Sister Nodes: 
..expandBerk-Tabatznik syndrome (C535432)
..expandFriedreich Ataxia, So-Called, with Optic Atrophy and Sensorineural Deafness (C564999)
..expandGrowth retardation, Alopecia, Pseudoanodontia and Optic atrophy (C535642)
..expandHagemoser Weinstein Bresnick syndrome (C537626)
..expandKonigsmark Knox Hussels syndrome (C537214)
..expandMetaphyseal Dysplasia, Anetoderma, and Optic Atrophy (C565395)
..expandNecrotizing Encephalomyelopathy, Subacute, of Leigh, Adult (C563530)
..expandOptic atrophy 1 and deafness (C537124)
..expandOptic Atrophy 4 (C565343)
..expandOptic atrophy 5 (C537126)
..expandOptic atrophy 6 (C537127)
..expandOptic Atrophy 7 (C567833)
..expandOptic atrophy and cataract, autosomal dominant (C537128)
..expandOptic atrophy polyneuropathy deafness (C537129)
..expandOptic Atrophy Spastic Paraplegia Syndrome (C564084)
..expandOptic Atrophy with Demyelinating Disease of CNS (C563496)
..expandOptic Atrophy with Negative Electroretinograms (C563494)
..expandOptic Atrophy, Autosomal Dominant (D029241)
..expandOptic Atrophy, Deafness, Ophthalmoplegia, and Myopathy (C565117)
..expandOptic Atrophy, Hereditary, Leber (D029242) Child1
..expandSenior Loken Syndrome (C537580)
..expandSenior-Loken Syndrome 3 (C564637)
..expandSenior-Loken Syndrome 5 (C563763)
..expandSenior-Loken Syndrome 6 (C565708)
..expandSpastic Paraplegia, Optic Atrophy, And Dementia (C566679)
..expandSpastic Paraplegia, Optic Atrophy, Microcephaly, And Xy Sex Reversal (C566409)
..expandWolfram Syndrome (D014929) Child1
..expandWolfram Syndrome, Mitochondrial Form (C564012)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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SELECT DISTINCT t2.disease_id, t2.disease_title, t.id AS HPO_ID1, t.acc as HPO_ID, t.name as HPO_Name , t5.frequency_modifier , o.comment AS Onset_name FROM hpo.external_object_disease AS t2, hpo.annotation AS t5 LEFT JOIN hpo.term AS t ON t.id = t5.term_id LEFT JOIN hpo.annotation_onset_modifier AS o ON o.annotation_id =t5.annotation_id WHERE t2.disease_id = '161700' AND t2.db_name='OMIM' AND t5.external_object_disease_id = t2.external_object_id ORDER BY HPO_Name like '%Auto%' DESC, HPO_Name like '%linked%' DESC, HPO_Name like '%onset%' DESC, HPO_Name, disease_title, t.name;
Term ID:7800
Name:Necrotizing Encephalomyelopathy, Subacute, of Leigh, Adult
Definition:
Alternative IDs:
ParentIDs:MESH:D007888|MESH:D015418
TreeNumbers:C10.228.140.163.100.412/C563530 |C10.292.700.225.500/C563530 |C10.574.500.662/C563530 |C11.270.564/C563530 |C11.640.451.451/C563530 |C16.320.290.564/C563530 |C16.320.400.630/C563530 |C16.320.565.189.412/C563530 |C16.320.565.202.810.444/C563530 |C18.452.132.100.41
Synonyms:Leigh Syndrome, Adult
Slim Mappings:Eye disease|Genetic disease (inborn)|Metabolic disease|Nervous system disease
Reference: MedGen: C563530
MeSH: C563530
OMIM: 161700;

Genes: