Human Phenotype Ontology 
Grandparent Node:
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Cephalocele (HP:0011815)help
Grandparent Node:
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Morphological central nervous system abnormality (HP:0002011)help
Parent Node:
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Encephalocele (HP:0002084)help
..Starting node
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Meningoencephalocele (HP:0006888)help
Term ID: 6888
Name: Meningoencephalocele
Synonym:
Definition:
Comments:
Reference: HP:0006888
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnterior basal encephalocele (HP:0006992) help
..expandAnterior encephalocele (HP:0007035) help
..expandBasal encephalocele (HP:0011817) help
..expandCranium bifidum occultum (HP:0004423) help
..expandFrontal encephalocele (HP:0007330) help
..expandOccipital encephalocele (HP:0002085) help
..expandOrbital encephalocele (HP:0007115) help
..expandParietal encephalocele (HP:0011816) help


Genes (5) :FKRP FKTN LARGE1 POMT1 POMT2

Diseases (1) :OMIM:236670
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.