Human Phenotype Ontology 
Grandparent Node:
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Morphological central nervous system abnormality (HP:0002011)help
Parent Node:
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Abnormal circulating copper concentration (HP:0010836)help
Parent Node:
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Abnormality of brain morphology (HP:0012443)help
..Starting node
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Copper accumulation in brain (HP:0012676)help
Term ID: 12676
Name: Copper accumulation in brain
Synonym: Brain copper accumulation; Copper accumulation in brain
Definition: An anomalous build up of copper (Cu) in the brain.
Comments:
Reference: HP:0012676
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal brainstem morphology (HP:0002363) help
..expandAbnormal cerebral vascular morphology (HP:0100659) help
..expandAbnormal cerebral ventricle morphology (HP:0002118) help
..expandAbnormal forebrain morphology (HP:0100547) help
..expandAbnormal hindbrain morphology (HP:0011282) help
..expandAbnormal midbrain morphology (HP:0002418) help
..expandAbnormal pineal morphology (HP:0012681) help
..expandAbnormality of the pituitary gland (HP:0012503) help
..expandHoloprosencephaly (HP:0001360) help
..expandIron accumulation in brain (HP:0012675) help
..expandKernicterus (HP:0001343) help
..expandobsolete Brain very small (HP:0001322) 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:0012676HP:0012676Copper accumulation in brain0 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.