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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: Hyperhidrosis (D006945)
Parent Node: Skin Diseases, Papulosquamous (D017444)
..Starting node ..Granulosis Rubra Nasi (C562483)
Child Nodes:
Sister Nodes:
..Comedones, Familial Dyskeratotic (C562838)
..Dermatitis, Seborrheic (D012628) 3
..Dermatosis Papulosa Nigra (C562379)
..dowling-degos disease (C562924)
..Granulosis Rubra Nasi (C562483)
..Lichenoid Eruptions (D017512) 8
..Parapsoriasis (D010267) 2
..Pityriasis (D010915) 5
..Psoriasis (D011565) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

4809

Name:

Granulosis Rubra Nasi

Definition:

Alternative IDs:

ParentIDs:

MESH:D006945|MESH:D017444

TreeNumbers:

C17.800.859/C562483 |C17.800.946.350/C562483

Synonyms:

Slim Mappings:

Skin disease

Reference:

MedGen: C562483
MeSH: C562483
OMIM: 139000;

Genes:

Phenotypes

1	HP:0000006	Autosomal dominant inheritance
2	HP:0011463	Childhood onset
3	HP:0000975	Hyperhidrosis

Disease Causing ClinVar Variants