Diaphragmatic hernia 2

Preferred Label : Diaphragmatic hernia 2;

Symbol : DIH2;

CISMeF acronym : DIH2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of congenital diaphragmatic hernia (CDH), see (DIH1; 142340).;

Inheritance : Autosomal recessive vs. multifactorial;

Prefixed ID : %222400;

Details

Origin ID

222400;

UMLS CUI

C1857284;

Broader ORDO disease(s)
- Congenital diaphragmatic hernia [ORDO Disease]
Currated CISMeF NLP mapping
- diaphragmatic hernia 2 [MeSH concept]
- diaphragmatic hernia 2 [MeSH Supplementary Concept]
DO Cross reference
- congenital diaphragmatic hernia [DO Concept]
HPO term(s)
- Agenesis of the diaphragm [HPO term]
- Autosomal recessive inheritance [HPO term]
- Congenital diaphragmatic hernia [HPO term]
- Multifactorial inheritance [HPO term]
ORDO concept(s)
- Congenital diaphragmatic hernia [ORDO Disease]
Semantic type(s)
- Anatomical Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- diaphragmatic hernia 2 [MeSH Supplementary Concept]
- diaphragmatic hernia 2 [MeSH concept]
Validated automatic mappings to NTBT
- Congenital diaphragmatic hernia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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