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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: Voice Disorders (D014832)
..Starting node ..Aphonia (D001044)
Child Nodes:
Sister Nodes:
..Aphonia (D001044)
..Dysphonia (D055154) 1
..Hoarseness (D006685) 2
..Whispering dysphonia, hereditary (C536698)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	815
Name:	Aphonia
Definition:	Complete loss of phonation due to organic disease of the larynx or to nonorganic (i.e., psychogenic) causes.
Alternative IDs:
ParentIDs:	MESH:D014832
TreeNumbers:	C08.360.940.160 \|C09.400.940.160 \|C10.597.975.100 \|C23.888.592.979.100
Synonyms:	Absence of Voice \|Aphonia, Functional \|Aphonia, Nonorganic \|Aphonia Paralytica \|Aphonias, Functional \|Aphonias, Nonorganic \|Aphonia, Spastic \|Aphonias, Spastic \|Functional Aphonia \|Functional Aphonias \|Nonorganic Aphonia \|Nonorganic Aphonias \|Paralytica, Aphonia \|Spa
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Respiratory tract disease\|Signs and symptoms
Reference:	MedGen: D001044 MeSH: D001044 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants