Human Phenotype Ontology 
Grandparent Node:
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Hypotonia (HP:0001252)help
Parent Node:
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Neonatal hypotonia (HP:0001319)help
..Starting node
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obsolete Severe neonatal hypotonia in males (HP:0006830)help
Term ID: 6830
Name: obsolete Severe neonatal hypotonia in males
Synonym:
Definition:
Comments:
Reference: HP:0006830
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGeneralized neonatal hypotonia (HP:0008935) 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:0006830HP:0006830obsolete Severe neonatal hypotonia in males0 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.