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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

Disease Browser
Parent Node: Laryngeal Diseases (D007818)
Parent Node: Paralysis (D010243)
Parent Node: Vagus Nerve Diseases (D020421)
..Starting node ..Vocal Cord Paralysis (D014826)
Child Nodes:
........CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE (OMIM:607706)
........Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy (C565252)
........Laryngeal Adductor Paralysis (C562861)
........Neuropathy, Distal Hereditary Motor, Type VIIA (C563562)
........Tucker syndrome (C536923)
........Vocal cord dysfunction familial (C536354)
Sister Nodes:
..Vagus Nerve Injuries (D061223) 2
..Vocal Cord Paralysis (D014826) 6
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11652
Name:	Vocal Cord Paralysis
Definition:	Congenital or acquired paralysis of one or both VOCAL CORDS. This condition is caused by defects in the CENTRAL NERVOUS SYSTEM, the VAGUS NERVE and branches of LARYNGEAL NERVES. Common symptoms are VOICE DISORDERS including HOARSENESS or APHONIA.
Alternative IDs:
ParentIDs:	MESH:D007818\|MESH:D010243\|MESH:D020421
TreeNumbers:	C08.360.931 \|C09.400.931 \|C10.292.887.800 \|C10.597.622.943 \|C23.888.592.636.943
Synonyms:	Acquired Vocal Cord Palsy \|Bilateral Vocal Cord Paresis \|Congenital Vocal Cord Palsy \|Laryngeal Nerve Palsy, Recurrent \|Laryngeal Paralyses \|Laryngeal Paralysis \|Palsies, Vocal Cord \|Palsies, Vocal Fold \|Palsy, Vocal Cord \|Palsy, Vocal Fold \|Paralyses, Laryngeal \|P
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Respiratory tract disease\|Signs and symptoms
Reference:	MedGen: D014826 MeSH: D014826 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants