Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Conjunctival Neoplasms (D003230)
Parent Node: Lipoma (D008067)
..Starting node ..Lipoma of the Conjunctiva (C563620)
Child Nodes:
Sister Nodes:
..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..Lipoblastoma (D062689)
..Lipoma of the Conjunctiva (C563620)
..LIPOMATOSIS, MULTIPLE (OMIM:151900)
..Lipomatous hemangiopericytoma (C537029)
..Median cleft lip, corpus callosum, lipoma, and skin polyps (C536135)
..Nasopalpebral lipoma coloboma syndrome (C538338)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

6477

Name:

Lipoma of the Conjunctiva

Definition:

Alternative IDs:

ParentIDs:

MESH:D003230|MESH:D008067

TreeNumbers:

C04.557.450.550.400/C563620 |C04.588.364.235/C563620 |C11.187.169/C563620 |C11.319.217/C563620

Synonyms:

Slim Mappings:

Cancer|Eye disease

Reference:

MedGen: C563620
MeSH: C563620
OMIM: 151700;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0012549	Conjunctival lipoma
3	HP:0012032	Lipoma

Disease Causing ClinVar Variants