Pica
Symptom Information:
| Symptom ID: | HPO:0011856 | ||||
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Abnormal eating behavior(HPO:0100738) Pica(HPO:0011856) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Appetite and general nutritional disorders(MedDRA:10003018) General nutritional disorders NEC(MedDRA:10018067) Pica(HPO:0011856) |
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| Database Frequency: | 1 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 17q12 microdeletion syndrome | (Orphanet:261265) |