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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: Cysts (D003560)
Parent Node: Teratoma (D013724)
..Starting node ..Dermoid Cyst (D003884)
Child Nodes:
........46,XX Gonadal dysgenesis epibulbar dermoid (C535316)
........Aplasia Cutis Congenita with Epibulbar Dermoids (C563969)
........Dermoid Cysts, Familial Frontonasal (C563455)
........Ring dermoid of cornea (C535684)
........Zadik Barak Levin syndrome (C536721)
Sister Nodes:
..Dermoid Cyst (D003884) 5
..Malignant Teratocarcinosarcoma (C535701)
..Nasopharyngeal teratoma with Dandy Walker diaphragmatic hernia (C538340)
..Pineal Teratoma (C537401)
..Sacral Agenesis Syndrome (C566762)
..Struma Ovarii (D013330)
..Teratoid Tumor, Atypical (C563737)
..Teratoma, Ovarian (C562731)
..Teratoma, Testicular (C562472)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	3245
Name:	Dermoid Cyst
Definition:	A tumor consisting of displaced ectodermal structures along the lines of embryonic fusion, the wall being formed of epithelium-lined connective tissue, including skin appendages, and containing keratin, sebum, and hair. (Stedman, 25th ed)
Alternative IDs:
ParentIDs:	MESH:D003560\|MESH:D013724
TreeNumbers:	C04.182.201 \|C04.557.465.910.250
Synonyms:	Cyst, Dermoid \|Cysts, Dermoid \|Dermoid \|Dermoid Cysts \|Dermoids
Slim Mappings:	Cancer
Reference:	MedGen: D003884 MeSH: D003884 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants