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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: Prune Belly Syndrome (D011535)
..Starting node ..Diastasis Recti And Weakness Of The Linea Alba (C567402)
Child Nodes:
Sister Nodes:
..Diastasis Recti And Weakness Of The Linea Alba (C567402)
..Prune Belly Syndrome with Pulmonic Stenosis, Mental Retardation, and Deafness (C562894)
..Urethral obstruction sequence (C536477)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

3347

Name:

Diastasis Recti And Weakness Of The Linea Alba

Definition:

Alternative IDs:

ParentIDs:

MESH:D011535

TreeNumbers:

C16.131.077.745/C567402

Synonyms:

Slim Mappings:

Congenital abnormality

Reference:

MedGen: C567402
MeSH: C567402
OMIM: 612198;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0009023	Abdominal wall muscle weakness
3	HP:0002019	Constipation
4	HP:0001540	Diastasis recti

Disease Causing ClinVar Variants