Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the spinal cord (HP:0002143)help
Parent Node:
expandMyelopathy (HP:0002196)help
..Starting node
..expandMyelocystocele (HP:0030709)help
Term ID: 30709
Name: Myelocystocele
Synonym:
Definition: Myelocystocele is characterized by a large, ependyma-lined, cystic dilation of the caudal end of the central canal of the spinal cord; it projects dorsally through a lamina defect, with overlying varying amounts of lipomatous subcutaneous tissue. Myelocystoceles are associated with a tethered cord and meningocele, which communicates with the spinal subarachnoid space, but not with the central canal cyst.
Comments:
Reference: HP:0030709
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCervical myelopathy (HP:0002318) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030709HP:0030709Myelocystocele0 CL E G H


Genes (0) :

Diseases (0) :
 

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