MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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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

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: bone cancer (MONDO:0002129)
Parent Node: larynx cancer (MONDO:0002352)
..Starting node ..laryngeal cartilage cancer ()
Child Nodes:
Sister Nodes:
..aryepiglottic fold cancer ()
..glottis cancer ()
..laryngeal carcinoma ()
..laryngeal cartilage cancer ()
..laryngeal sarcoma ()
..subglottis cancer ()
..supraglottis cancer ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1691
Name:	laryngeal cartilage cancer
Definition:	A malignant neoplasm involving the laryngeal cartilage.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	cancer of laryngeal cartilage; laryngeal cartilage cancer; malignant laryngeal cartilage neoplasm; malignant neoplasm of laryngeal cartilage; malignant neoplasm of laryngeal cartilages; malignant tumor of laryngeal cartilage
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal