Human Phenotype Ontology 
Grandparent Node:
expandAbnormal myocardium morphology (HP:0001637)help
Grandparent Node:
expandAmyloidosis (HP:0011034)help
Parent Node:
expandCardiac amyloidosis (HP:0030843)help
..Starting node
..expandMonoclonal light chain cardiac amyloidosis (HP:0031326)help
Term ID: 31326
Name: Monoclonal light chain cardiac amyloidosis
Synonym:
Definition: A type of cardiac amyloidosis related to deposition of an immunoglobulin light chain. The current gold standard of amyloid typing is to determine the precursor protein using laser microdissection mass spectrometry.
Comments:
Reference: HP:0031326
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandTransthyretin cardiac amyloidosis (HP:0031327) 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:0031326HP:0031326Monoclonal light chain cardiac amyloidosis0 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.