H19/igf2-imprinting control region

Preferred Label : H19/igf2-imprinting control region;

Type : Gene;

Alternative titles and symbols : H19 icr; ICR1;

Prefixed ID : *616186;

Details

Origin ID

616186;

UMLS CUI

C1415847;

Phenotypes related
- Beckwith-wiedemann syndrome [OMIM Phenotype]
- Silver-russell syndrome 1 [OMIM Phenotype]
- Wilms tumor 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythroderma [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients