Diaphragmatic hernia 3

Preferred Label : Diaphragmatic hernia 3;

Symbol : DIH3;

CISMeF acronym : DIH3;

Type : Phenotype, molecular basis known;

Prefixed ID : #610187;

Details

Origin ID

610187;

UMLS CUI

C1857781;

Automatic exact mappings (from CISMeF team)
- ZFPM2 wt Allele [NCIt concept]
Broader ORDO disease(s)
- Congenital diaphragmatic hernia [ORDO Disease]
Currated CISMeF NLP mapping
- diaphragmatic hernia 3 [MeSH concept]
- diaphragmatic hernia 3 [MeSH Supplementary Concept]
DO Cross reference
- congenital diaphragmatic hernia [DO Concept]
Genes related to phenotype
- Zinc finger protein, fog family member 2 [OMIM gene]
HPO term(s)
- Congenital diaphragmatic hernia [HPO term]
ORDO concept(s)
- Congenital diaphragmatic hernia [ORDO Disease]
Semantic type(s)
- Anatomical Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- diaphragmatic hernia 3 [MeSH Supplementary Concept]
- diaphragmatic hernia 3 [MeSH concept]
Validated automatic mappings to NTBT
- Congenital diaphragmatic hernia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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