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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: Hernia, Hiatal (D006551)
Parent Node: Microcephaly (D008831)
Parent Node: Nephrosis (D009401)
..Starting node ..Galloway Mowat syndrome (C537548)
Child Nodes:
Sister Nodes:
..Barakat syndrome (C537907)
..FORSYTHE-WAKELING SYNDROME (OMIM:613606)
..Galloway Mowat syndrome (C537548)
..Nephrosialidosis (C562606)
..Nephrosis deafness urinary tract digital malformation (C536402)
..Nephrosis, Lipoid (D009402)
..Nephrotic Syndrome (D009404) 14
..Pulmonic Stenosis and Congenital Nephrosis (C562895)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	4484
Name:	Galloway Mowat syndrome
Definition:
Alternative IDs:
ParentIDs:	MESH:D006551\|MESH:D008831\|MESH:D009401
TreeNumbers:	C05.660.207.620/C537548 \|C10.500.507.400.500/C537548 \|C12.777.419.630/C537548 \|C13.351.968.419.630/C537548 \|C16.131.621.207.620/C537548 \|C16.131.666.507.400.500/C537548 \|C23.300.707.500.467/C537548
Synonyms:	Galloway-Mowat Syndrome \|Galloway syndrome \|Microcephaly, hiatal hernia and nephrotic syndrome \|Microcephaly, Hiatus Hernia, And Nephrotic Syndrome \|Microcephaly nephrosis syndrome \|Nephrosis-Microcephaly Syndrome \|Nephrosis neuronal dysmigration syndrome \|Neph
Slim Mappings:	Congenital abnormality\|Musculoskeletal disease\|Nervous system disease\|Pathology (anatomical condition)\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C537548 MeSH: C537548 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants