Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormality of higher mental function (HP:0011446)help
..Starting node
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Micrographia (HP:0031908)help
Term ID: 31908
Name: Micrographia
Synonym:
Definition: Abnormally small sized handwriting defined formally as an impairment of a fine motor skill manifesting mainly as a progressive or stable reduction in amplitude during a writing task.
Comments:
Reference: HP:0031908
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgnosia (HP:0010524) help
..expandApraxia (HP:0002186) help
..expandCognitive impairment (HP:0100543) help
..expandLanguage impairment (HP:0002463) help
..expandNeurological speech impairment (HP:0002167) help
..expandOptic ataxia (HP:0031868) help
..expandReduced consciousness/confusion (HP:0004372) 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:0031908HP:0031908Micrographia0ADH1C CL E G H126251OMIM:168600Parkinson disease, late-onset.4
HP:0031908HP:0031908Micrographia0ATXN2 CL E G H631110555OMIM:168600Parkinson disease, late-onset.11
HP:0031908HP:0031908Micrographia0ATXN8OS CL E G H631510561OMIM:168600Parkinson disease, late-onset.1
HP:0031908HP:0031908Micrographia0FTL CL E G H25123999OMIM:606159Neurodegeneration with brain iron accumulation 3.33
HP:0031908HP:0031908Micrographia0GBA1 CL E G H26294177OMIM:168600Parkinson disease, late-onset.
HP:0031908HP:0031908Micrographia0GLUD2 CL E G H27474336OMIM:168600Parkinson disease, late-onset.1
HP:0031908HP:0031908Micrographia0MAPT CL E G H41376893OMIM:168600Parkinson disease, late-onset.140
HP:0031908HP:0031908Micrographia0MAPT CL E G H41376893ORPHA:240094Progressive supranuclear palsy-pure akinesia with gait freezing syndromeHP:0040282 - Frequent140
HP:0031908HP:0031908Micrographia0MAPT CL E G H41376893OMIM:601104Supranuclear palsy, progressive, 1140
HP:0031908HP:0031908Micrographia0NR4A2 CL E G H49297981OMIM:168600Parkinson disease, late-onset.27
HP:0031908HP:0031908Micrographia0PDGFB CL E G H51558800OMIM:213600Basal ganglia calcification, idiopathic, 1.9
HP:0031908HP:0031908Micrographia0PDGFRB CL E G H51598804OMIM:213600Basal ganglia calcification, idiopathic, 1.28
HP:0031908HP:0031908Micrographia0SLC20A2 CL E G H657510947OMIM:213600Basal ganglia calcification, idiopathic, 1.70
HP:0031908HP:0031908Micrographia0SNCA CL E G H662211138OMIM:168601Parkinson disease 1, autosomal dominant.65
HP:0031908HP:0031908Micrographia0SNCAIP CL E G H962711139OMIM:168600Parkinson disease, late-onset.35
HP:0031908HP:0031908Micrographia0TBP CL E G H690811588OMIM:168600Parkinson disease, late-onset.7
HP:0031908HP:0031908Micrographia0TRNT CL E G H45767499OMIM:168600Parkinson disease, late-onset.
HP:0031908HP:0031908Micrographia0VPS13A CL E G H232301908ORPHA:2388ChoreoacanthocytosisHP:0040283 - Occasional130


Genes (16) :ADH1C ATXN2 ATXN8OS FTL GBA1 GLUD2 MAPT NR4A2 PDGFB PDGFRB SLC20A2 SNCA SNCAIP TBP TRNT VPS13A

Diseases (7) :OMIM:168600 OMIM:606159 ORPHA:240094 OMIM:601104 OMIM:213600 OMIM:168601 ORPHA:2388
 

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