encephalocele - CISMeF

Preferred Label : encephalocele;

MeSH definition : Brain tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur.;

MeSH synonym : cerebral hernias; cerebral hernia; encephaloceles; hernia, cerebral; hernias, cerebral; cephalocele; cephaloceles; cranial meningoencephalocele; cranial meningoencephaloceles; meningoencephalocele, cranial; meningoencephaloceles, cranial; cranium bifidum; bifidum, cranium; bifidums, cranium; cranium bifidums; bifid cranium; bifid craniums; cranium, bifid; craniums, bifid; craniocele; cranioceles;

MeSH hyponym : encephalocele, sincipital; frontal encephalocele; occipital encephalocele; acquired encephalocele; Encephaloceles, Frontal; Frontal Encephaloceles; Encephalocele, Frontal; Acquired Encephaloceles; Encephaloceles, Acquired; Encephalocele, Acquired; Encephaloceles, Sincipital; Sincipital Encephaloceles; Sincipital Encephalocele; Encephaloceles, Occipital; Occipital Encephaloceles; Notoencephalocele; Notoencephaloceles; Encephalocele, Occipital;

Related MeSH term : cerebellar herniation; Cerebellar Herniations; Herniation, Cerebellar; Herniations, Cerebellar; Tonsillar Hernia; Hernia, Tonsillar; Hernias, Tonsillar; Tonsillar Hernias; Tonsillar Herniation; Herniation, Tonsillar; Herniations, Tonsillar; Tonsillar Herniations; Cerebellar Hernia; Cerebellar Hernias; Hernia, Cerebellar; Hernias, Cerebellar;

MeSH annotation : meningoencephalocele: coordinate IM with MENINGOCELE (IM);

Wikipedia link : https://en.wikipedia.org/wiki/Encephalocele;

Details

Origin ID

D004677;

UMLS CUI

C0014065;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Acquired encephalocele [MedDRA Preferred Term]
- Anterior encephalocele [HPO term]
- Brain herniation [MedDRA Preferred Term]
- Cerebellar hernia (disorder) [SNOMED CT concept]
- Cranioschisis (disorder) [SNOMED CT concept]
- Encephalocele [ACR pathology]
- Encephalocele [ACR pathology]
- Encephalocele, unspecified [ICD-10 Sub-category (who)]
- Frontal encephalocele [ICD-10 Sub-category]
- Frontal encephalocele [ICD-10 Sub-category (who)]
- Frontal encephalocele [HPO term]
- Frontal encephalocele [ORDO Disease]
- Frontal encephalocele (disorder) [SNOMED CT concept]
- Hernia of cerebellar tonsil into foramen magnum (disorder) [SNOMED CT concept]
- Parietal foramina [ICD-11 More detail]
- cerebral herniation [Radlex concept]
Currated CISMeF NLP mapping
- Cephalocele [HPO term]
- Cephalocele [ICD-11 Category]
- Cephalocele [ORDO Disease]
- Cerebral herniation (disorder) [SNOMED CT concept]
- Congenital cerebral hernia (disorder) [SNOMED CT concept]
- ENCEPHALOCELE [WHO-ART Preferred Term]
- Encephalocele [ICD-10 category]
- Encephalocele [PASCAL descriptor]
- Encephalocele [ICD-9 code]
- Encephalocele [ICD-10 category (who)]
- Encephalocele [MedDRA Preferred Term]
- Encephalocele [ICD-11 More detail]
- Encephalocele [NCIt concept]
- Encephalocele [HPO term]
- Encephalocele (disorder) [SNOMED CT concept]
- Encephalocele, unspecified [ICD-10 Sub-category]
- Isolated encephalocele [ORDO Disease]
- Occipital encephalocele [HPO term]
- Occipital encephalocele [ORDO Disease]
- Occipital encephalocele (disorder) [SNOMED CT concept]
- cerebral herniation [SNOMED Notion]
- encephalocele [Disease (Nov.)]
- encephalocele, nos [SNOMED Notion]
- occipital encephalocele [SNOMED Notion]
HPO term
- Cephalocele [HPO term]
- Encephalocele [HPO term]
- Frontal encephalocele [HPO term]
- Occipital encephalocele [HPO term]
Manual NTBT mappings (CISMeF)
- Non-syndromic central nervous system malformation [ORDO Disease]
ORDO relation(s)
- Isolated encephalocele [ORDO Disease]
Record concept(s)
- acquired encephalocele [MeSH concept]
- cerebellar herniation [MeSH concept]
- encephalocele [MeSH concept]
- encephalocele, sincipital [MeSH concept]
- frontal encephalocele [MeSH concept]
- occipital encephalocele [MeSH concept]
Related MeSH Supplementary Concept(s)
- DK phocomelia syndrome [MeSH Supplementary Concept]
- Dandy-Walker malformation with occipital cephalocele, autosomal dominant [MeSH Supplementary Concept]
- Meckel-Like cerebrorenodigital syndrome [MeSH Supplementary Concept]
- Podder-Tolmie syndrome [MeSH Supplementary Concept]
- Zechi-Ceide syndrome [MeSH Supplementary Concept]
- cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome [MeSH Supplementary Concept]
- cerebrorenodigital syndrome with limb malformations and triradiate acetabula [MeSH Supplementary Concept]
- fronto-facio-nasal dysplasia [MeSH Supplementary Concept]
- knobloch syndrome [MeSH Supplementary Concept]
- knobloch syndrome type II [MeSH Supplementary Concept]
- knobloch syndrome type III [MeSH Supplementary Concept]
- laryngeal atresia, encephalocele, and limb deformities [MeSH Supplementary Concept]
- meckel syndrome type 1 [MeSH Supplementary Concept]
- meckel syndrome type 2 [MeSH Supplementary Concept]
- meckel syndrome type 3 [MeSH Supplementary Concept]
- meckel syndrome, type 4 [MeSH Supplementary Concept]
- meckel syndrome, type 5 [MeSH Supplementary Concept]
- meckel syndrome, type 6 [MeSH Supplementary Concept]
- parietal foramina [MeSH Supplementary Concept]
- parietal foramina 1 [MeSH Supplementary Concept]
- parietal foramina 2 [MeSH Supplementary Concept]
- parietal foramina 3 [MeSH Supplementary Concept]
- parietal foramina with cleidocranial dysplasia [MeSH Supplementary Concept]
- sakoda complex [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Cerebellar hernia (disorder) [SNOMED CT concept]
- cranioschisis [Disease (Nov.)]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cephalocele [ORDO Disease]
- Cephalocele [HPO term]
- Congenital cerebral hernia (disorder) [SNOMED CT concept]
- ENCEPHALOCELE [WHO-ART Preferred Term]
- Encephalocele [ICD-10 category (who)]
- Encephalocele [HPO term]
- Isolated encephalocele [ORDO Disease]
- encephalocele, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Frontal encephalocele [ICD-11 More detail]
- Frontal encephalocele (disorder) [SNOMED CT concept]
- Occipital encephalocele [ICD-10 Sub-category]
- Occipital encephalocele [ICD-11 More detail]
- Occipital encephalocele [ICD-10 Sub-category (who)]

Keyword's position in hierarchy(ies) :

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