Human Phenotype Ontology 
Grandparent Node:
expandMorphological central nervous system abnormality (HP:0002011)help
Parent Node:
expandAbnormality of brain morphology (HP:0012443)help
..Starting node
..expandobsolete Brain very small (HP:0001322)help
Term ID: 1322
Name: obsolete Brain very small
Synonym:
Definition:
Comments:
Reference: HP:0001322
Genes and Diseases:
 
       Child Nodes:
........expandBrain atrophy (HP:0012444) help
................... HP:0002283 Global brain atrophy
................... HP:0007369 Atrophy/Degeneration affecting the cerebrum
................... HP:0007374 Atrophy/Degeneration involving the caudate nucleus

 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
..expandCopper accumulation in brain (HP:0012676) help
..expandHoloprosencephaly (HP:0001360) help
..expandIron accumulation in brain (HP:0012675) help
..expandKernicterus (HP:0001343) 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:0001322HP:0001322obsolete Brain very small0 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.