Human Phenotype Ontology / 人类表型本体

Last uploaded: September 7, 2023
Preferred Name

Cephalocele

Definitions

A congenital defect in the skull, whereby there is a protrusion of part of the cranial contents through a congenital defect in the cranium, usually covered with skin or mucous membrane. The term encephalocele refers to a subclass of these lesions in which brain tissue protrudes through the defect. A cephalocele is a rare birth defect that is characterized by a sac-like mass protruding through a defective opening in the skull. The sac varies in size that typically consists of herniated meninges and brain tissue (meningoencephalocele or encephalocele) or fragments of disorganized neural tissue. Alternatively, the sac may contain only the meninges (cranial meningocele) or it may include part of the ventricle filled with CSF (encephalocystocele) covered by skin (from PMID:24931720).

ID

http://purl.obolibrary.org/obo/HP_0011815

comment

A cephalocele is a rare birth defect that is characterized by a sac-like mass protruding through a defective opening in the skull. The sac varies in size that typically consists of herniated meninges and brain tissue (meningoencephalocele or encephalocele) or fragments of disorganized neural tissue. Alternatively, the sac may contain only the meninges (cranial meningocele) or it may include part of the ventricle filled with CSF (encephalocystocele) covered by skin (from PMID:24931720).

creation_date

2012-04-29T09:04:09Z

creator

https://orcid.org/0000-0002-0736-9199

database_cross_reference

SNOMEDCT_US:48777005

SNOMEDCT_US:253101008

MSH:D004677

SNOMEDCT_US:55999004

UMLS:C0014065

definition

A congenital defect in the skull, whereby there is a protrusion of part of the cranial contents through a congenital defect in the cranium, usually covered with skin or mucous membrane. The term encephalocele refers to a subclass of these lesions in which brain tissue protrudes through the defect.

has_obo_namespace

human_phenotype

id

HP:0011815

label

Cephalocele

notation

HP:0011815

prefLabel

Cephalocele

treeView

http://purl.obolibrary.org/obo/HP_0000929

subClassOf

http://purl.obolibrary.org/obo/HP_0000929

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0017078 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0017078 Experimental Factor Ontology / 实验性因素本体 LOOM
http://www.orpha.net/ORDO/Orphanet_268817 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/LA01 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM