MSeqDR Mitochondrial Disease Portal


 
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Disease Browser
Parent Node:
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Heredodegenerative Disorders, Nervous System (D020271)
Parent Node:
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Liver Diseases (D008107)
Parent Node:
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Mitochondrial Diseases (D028361)
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Peripheral Nervous System Diseases (D010523)
..Starting node
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Navajo neurohepatopathy (C538344)

       Child Nodes:
........expandMITOCHONDRIAL DNA DEPLETION SYNDROME 6 (HEPATOCEREBRAL TYPE) (OMIM:256810)  LSDB  L: 00035;



 Sister Nodes: 
..expandAccessory deep peroneal nerve (C536001)
..expandAcrodynia (D000170)
..expandAmyloid Neuropathies (D017772) Child3
..expandBrachial Plexus Neuropathies (D020516) Child4
..expandCataract ataxia deafness (C538283)
..expandComplex Regional Pain Syndromes (D020918) Child2
..expandCorpus callosum agenesis neuronopathy (C536446)
..expandDeafness, X-Linked 5 (C564472)
..expandDiabetic Neuropathies (D003929) Child2
..expandGiant Axonal Neuropathy (D056768) Child1
..expandGuillain-Barre Syndrome (D020275) Child1
..expandHand-Arm Vibration Syndrome (D053421)
..expandHypertrophic Neuropathy And Cataract (C565490)
..expandInherited Peripheral Neuropathy (C548028)
..expandIsaacs Syndrome (D020386)
..expandMononeuropathies (D020422) Child15
..expandNavajo neurohepatopathy (C538344) Child1  LSDB C:1
..expandNerve Compression Syndromes (D009408) Child13
..expandNeuralgia (D009437) Child6
..expandNeuritis (D009443) Child3
..expandNeurofibromatosis 1 (D009456) Child1
..expandNEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC (OMIM:613376)
..expandNeuropathy, Painful (C564945)
..expandNeuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine (C563516)
..expandOptic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
..expandPain Insensitivity, Congenital (D000699) Child2
..expandPeripheral Nerve Injuries (D059348)
..expandPeripheral Nervous System Neoplasms (D010524) Child25  LSDB C:1
..expandPeripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (C564894)
..expandPolyneuropathies (D011115) Child200  LSDB C:3
..expandRadiculopathy (D011843)
..expandSacral plexopathy (C537224)
..expandSpinocerebellar Ataxia With Rigidity And Peripheral Neuropathy (C566669)
..expandTarlov Cysts (D052958)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:7787
Name:Navajo neurohepatopathy
Definition:
Alternative IDs:
ParentIDs:MESH:D008107|MESH:D010523|MESH:D020271|MESH:D028361
TreeNumbers:C06.552/C538344 |C10.574.500/C538344 |C10.668.829/C538344 |C16.320.400/C538344 |C18.452.660/C538344
Synonyms:Mitochondrial Dna Depletion Syndrome 6 |MPV17-Associated Hepatocerebral MDS |MPV17-Related Hepatocerebral Mitochondrial DNA Depletion Syndrome |MTDPS6 |Navajo Familial Neurogenic Arthropathy |Navajo neuropathy
Slim Mappings:Digestive system disease|Genetic disease (inborn)|Metabolic disease|Nervous system disease
Reference: MedGen: C538344
MeSH: C538344
OMIM:
MSeqDR LSDB:
MSeqDR has 1 matches in descendants: 00035;  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal