Neural tube defects, X-linked

Preferred Label : Neural tube defects, X-linked;

Type : Other, mainly phenotypes with suspected mendelian basis;

Included titles and symbols : Spina bifida, X-linked;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of neural tube defects, see 182940 and 601634.;

Inheritance : X-linked form;

Prefixed ID : 301410;

Details

Origin ID

301410;

UMLS CUI

C1845026;

Automatic exact mappings (from CISMeF team)
- Neural tube closure defect [ORDO Disease]
- neural tube defects X-linked [MeSH Supplementary Concept]
- neural tube defects X-linked [MeSH concept]
- spina bifida, X-Linked [MeSH Supplementary Concept]
- spina bifida, X-Linked [MeSH concept]
DO Cross reference
- neural tube defect [DO Concept]
HPO term(s)
- Anencephaly [HPO term]
- Spina bifida [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- Isolated spina bifida [ORDO Disease]
- Neural tube closure defect [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- neural tube defects X-linked [MeSH Supplementary Concept]
- neural tube defects X-linked [MeSH concept]

Keyword's position in hierarchy(ies) :

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