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: Intellectual Disability (D008607)
Parent Node: Psoriasis (D011565)
..Starting node ..Mental Retardation associated with Psoriasis (C564107)
Child Nodes:
Sister Nodes:
..Arthritis, Psoriatic (D015535)
..Mental Retardation associated with Psoriasis (C564107)
..Tranebjaerg Svejgaard syndrome (C536978)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

6972

Name:

Mental Retardation associated with Psoriasis

Definition:

Alternative IDs:

ParentIDs:

MESH:D008607|MESH:D011565

TreeNumbers:

C10.597.606.643/C564107 |C17.800.859.675/C564107 |C23.888.592.604.646/C564107 |F03.550.600/C564107

Synonyms:

Slim Mappings:

Mental disorder|Nervous system disease|Signs and symptoms|Skin disease

Reference:

MedGen: C564107
MeSH: C564107
OMIM: 309480;

Genes:

Phenotypes

Disease Causing ClinVar Variants