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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: Eye Neoplasms (D005134)
Parent Node: Eyelid Diseases (D005141)
Parent Node: Facial Neoplasms (D005153)
..Starting node ..Eyelid Neoplasms (D005142)
Child Nodes:
........Nasopalpebral lipoma coloboma syndrome (C538338)
........Schopf-Schulz-Passarge Syndrome (C565607)
Sister Nodes:
..Eyelid Neoplasms (D005142) 2
..Supraumbilical midabdominal raphe and facial cavernous hemangiomas (C538144)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4060
Name:	Eyelid Neoplasms
Definition:	Tumors of cancer of the EYELIDS.
Alternative IDs:
ParentIDs:	MESH:D005134\|MESH:D005141\|MESH:D005153
TreeNumbers:	C04.588.443.392.500 \|C11.319.421 \|C11.338.526
Synonyms:	Eyelid Neoplasm \|Neoplasm, Eyelid \|Neoplasms, Eyelid
Slim Mappings:	Cancer\|Eye disease
Reference:	MedGen: D005142 MeSH: D005142 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants