Disease browser and phenotype portal

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MSeqDR-LSDB
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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

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: Peripheral Nervous System Diseases (D010523)
..Starting node ..Nerve Compression Syndromes (D009408)
Child Nodes:
........Carpal Tunnel Syndrome (D002349)
........Meralgia Paraesthetica, Familial (C563590)
........Meralgia paresthetica (C537458)
........Piriformis Muscle Syndrome (D055958) 1
........Pudendal Neuralgia (D060545)
........Superior Transverse Scapular Ligament, Calcification Of, Familial (C566638)
........Tarsal Tunnel Syndrome (D013641)
........Thoracic Outlet Syndrome (D013901) 2
........Ulnar Nerve Compression Syndromes (D017769) 1
Sister Nodes:
..Accessory deep peroneal nerve (C536001)
..Acrodynia (D000170)
..Amyloid Neuropathies (D017772) 3
..Brachial Plexus Neuropathies (D020516) 4
..Cataract ataxia deafness (C538283)
..Complex Regional Pain Syndromes (D020918) 2
..Corpus callosum agenesis neuronopathy (C536446)
..Deafness, X-Linked 5 (C564472)
..Diabetic Neuropathies (D003929) 2
..Giant Axonal Neuropathy (D056768) 1
..Guillain-Barre Syndrome (D020275) 1
..Hand-Arm Vibration Syndrome (D053421)
..Hypertrophic Neuropathy And Cataract (C565490)
..Inherited Peripheral Neuropathy (C548028)
..Isaacs Syndrome (D020386)
..Mononeuropathies (D020422) 15
..Navajo neurohepatopathy (C538344) 1
..Nerve Compression Syndromes (D009408) 13
..Neuralgia (D009437) 6
..Neuritis (D009443) 3
..Neurofibromatosis 1 (D009456) 1
..NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC (OMIM:613376)
..Neuropathy, Painful (C564945)
..Neuropathy, with Paraprotein in Serum, Cerebrospinal Fluid and Urine (C563516)
..Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
..Pain Insensitivity, Congenital (D000699) 2
..Peripheral Nerve Injuries (D059348)
..Peripheral Nervous System Neoplasms (D010524) 25
..Peripheral Neuropathy, Ataxia, Focal Necrotizing Encephalopathy, and Spongy Degeneration of Brain (C564894)
..Polyneuropathies (D011115) 200
..Radiculopathy (D011843)
..Sacral plexopathy (C537224)
..Spinocerebellar Ataxia With Rigidity And Peripheral Neuropathy (C566669)
..Tarlov Cysts (D052958)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	7905
Name:	Nerve Compression Syndromes
Definition:	Mechanical compression of nerves or nerve roots from internal or external causes. These may result in a conduction block to nerve impulses (due to MYELIN SHEATH dysfunction) or axonal loss. The nerve and nerve sheath injuries may be caused by ISCHEMIA; INFLAMMATION; or a direct mechanical effect.
Alternative IDs:
ParentIDs:	MESH:D010523
TreeNumbers:	C10.668.829.550
Synonyms:	Compression Syndrome, Nerve \|Compression Syndromes, Nerve \|Entrapment, Nerve \|Entrapment Neuropathies \|Entrapments, Nerve \|External Nerve Compression Syndromes \|Internal Nerve Compression Syndromes \|Nerve Compression Syndrome \|Nerve Compression Syndromes, Extern
Slim Mappings:	Nervous system disease
Reference:	MedGen: D009408 MeSH: D009408 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants