Human Phenotype Ontology 
Grandparent Node:
expandAbnormal consumption behavior (HP:0040202)help
Parent Node:
expandAbnormal eating behavior (HP:0100738)help
..Starting node
..expandPica (HP:0011856)help
Term ID: 11856
Name: Pica
Synonym:
Definition: An appetite for and the persistent ingestion of non-food substances such as clay. In order to diagnose pica, this behavior must have persisted over a period of at least one month.
Comments:
Reference: HP:0011856
Genes and Diseases:
 
       Child Nodes:
........expandGeophagia (HP:0025062) help

 Sister Nodes: 
..expandBulimia (HP:0100739) help
..expandChoking episodes (HP:0030842) help
..expandOral aversion (HP:0012523) help
..expandPolyphagia (HP:0002591) help
..expandSalt craving (HP:0030083) help
..expandSweet craving (HP:0030221) 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:0011856HP:0011856Pica0ASH1L CL E G H5587019088OMIM:617796Mental retardation, autosomal dominant 521
HP:0011856HP:0011856Pica0CDK13 CL E G H86211733OMIM:617360Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder8
HP:0011856HP:0011856Pica0CHD8 CL E G H5768020153OMIM:615032AUTISM, SUSCEPTIBILITY TO, 18; AUTS1872
HP:0011856HP:0011856Pica0DHPS CL E G H17252869OMIM:618480Neurodevelopmental disorder with seizures and speech and walking impairment.
HP:0011856HP:0011856Pica0ELP2 CL E G H5525018248OMIM:617270Mental retardation, autosomal recessive 586
HP:0011856HP:0025062Geophagia1 CL E G H


Genes (5) :ASH1L CDK13 CHD8 DHPS ELP2

Diseases (5) :OMIM:617796 OMIM:617360 OMIM:615032 OMIM:618480 OMIM:617270
 

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