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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: Sensation Disorders (D012678)
..Starting node ..Olfaction Disorders (D000857)
Child Nodes:
........Congenital anosmia (C535983)
........Johnson neuroectodermal syndrome (C535882)
........Musk, Inability to Smell (C564980)
........Neuropathy, Hereditary Sensory and Autonomic, Adult-Onset, with Anosmia (C563870)
Sister Nodes:
..Dizziness (D004244) 1
..Hearing Disorders (D006311) 403
..Olfaction Disorders (D000857) 4
..Posterior column ataxia (C536342)
..Somatosensory Disorders (D020886) 6
..Taste Disorders (D013651) 3
..Vision Disorders (D014786) 84
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	8213
Name:	Olfaction Disorders
Definition:	Loss of or impaired ability to smell. This may be caused by OLFACTORY NERVE DISEASES; PARANASAL SINUS DISEASES; viral RESPIRATORY TRACT INFECTIONS; CRANIOCEREBRAL TRAUMA; SMOKING; and other conditions.
Alternative IDs:
ParentIDs:	MESH:D012678
TreeNumbers:	C10.597.751.600 \|C23.888.592.763.550
Synonyms:	Anosmia \|Cacosmia \|Cacosmias \|Dysosmia \|Dysosmias \|Olfaction Disorder \|Paraosmia \|Paraosmias \|Smell Disorder \|Smell Disorders
Slim Mappings:	Nervous system disease\|Signs and symptoms
Reference:	MedGen: D000857 MeSH: D000857 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants