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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: Genetic Diseases, X-Linked (D040181)
Parent Node: Glomerulonephritis, Membranoproliferative (D015432)
..Starting node ..Membranoproliferative Glomerulonephritis, X-Linked (C564423)
Child Nodes:
Sister Nodes:
..Glomerulonephritis sparse hair telangiectases (C536825)
..Glomerulonephritis With Isolated C3 Deposits And Factor H Deficiency (C566939)
..Glomerulonephritis With Isolated C3 Deposits And Factor I Deficiency (C567033)
..Glomerulopathy with fibronectin deposits (C536826)
..Membranoproliferative Glomerulonephritis, X-Linked (C564423)
..MPGN II with Complement Factor H Deficiency (C566938)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

6934

Name:

Membranoproliferative Glomerulonephritis, X-Linked

Definition:

Alternative IDs:

OMIM:305800

ParentIDs:

MESH:D015432|MESH:D040181

TreeNumbers:

C12.777.419.570.363.615/C564423 |C13.351.968.419.570.363.615/C564423 |C16.320.322/C564423 |C20.425/C564423

Synonyms:

Mesangiocapillary Glomerulonephritis, X-Linked

Slim Mappings:

Genetic disease (inborn)|Immune system disease|Urogenital disease (female)|Urogenital disease (male)

Reference:

MedGen: C564423
MeSH: C564423
OMIM: 305800;

Genes:

Phenotypes

1	HP:0001939	Abnormality of metabolism/homeostasis
2	HP:0001693	Cardiac shunt
3	HP:0009125	Lipodystrophy
4	HP:0000793	Membranoproliferative glomerulonephritis

Disease Causing ClinVar Variants