Human Phenotype
Ontology
Grandparent Node: Abnormal nervous system physiology (HP:0012638) Parent Node: Abnormality of higher mental function (HP:0011446) ..Starting node .. Micrographia (HP:0031908)
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: ..Agnosia (HP:0010524) ..Apraxia (HP:0002186) ..Cognitive impairment (HP:0100543) ..Language impairment (HP:0002463) ..Neurological speech impairment (HP:0002167) ..Optic ataxia (HP:0031868) ..Reduced consciousness/confusion (HP:0004372) Input HPO ID HPO term Distance Gene Gene id entrez HGNC ID DiseaseId DiseaseName Frequency Onset HGMD variants ClinVar variants HPO disease - gene - phenotype typical associations: HPO disease - gene - phenotype less frequent non-typical associations: HP:0031908 HP:0031908 Micrographia 0 ADH1C CL E G H 126 251 OMIM:168600 Parkinson disease, late-onset . 4 HP:0031908 HP:0031908 Micrographia 0 ATXN2 CL E G H 6311 10555 OMIM:168600 Parkinson disease, late-onset . 11 HP:0031908 HP:0031908 Micrographia 0 ATXN8OS CL E G H 6315 10561 OMIM:168600 Parkinson disease, late-onset . 1 HP:0031908 HP:0031908 Micrographia 0 FTL CL E G H 2512 3999 OMIM:606159 Neurodegeneration with brain iron accumulation 3 . 33 HP:0031908 HP:0031908 Micrographia 0 GBA1 CL E G H 2629 4177 OMIM:168600 Parkinson disease, late-onset . HP:0031908 HP:0031908 Micrographia 0 GLUD2 CL E G H 2747 4336 OMIM:168600 Parkinson disease, late-onset . 1 HP:0031908 HP:0031908 Micrographia 0 MAPT CL E G H 4137 6893 OMIM:168600 Parkinson disease, late-onset . 140 HP:0031908 HP:0031908 Micrographia 0 MAPT CL E G H 4137 6893 ORPHA:240094 Progressive supranuclear palsy-pure akinesia with gait freezing syndrome HP:0040282 - Frequent 140 HP:0031908 HP:0031908 Micrographia 0 MAPT CL E G H 4137 6893 OMIM:601104 Supranuclear palsy, progressive, 1 140 HP:0031908 HP:0031908 Micrographia 0 NR4A2 CL E G H 4929 7981 OMIM:168600 Parkinson disease, late-onset . 27 HP:0031908 HP:0031908 Micrographia 0 PDGFB CL E G H 5155 8800 OMIM:213600 Basal ganglia calcification, idiopathic, 1 . 9 HP:0031908 HP:0031908 Micrographia 0 PDGFRB CL E G H 5159 8804 OMIM:213600 Basal ganglia calcification, idiopathic, 1 . 28 HP:0031908 HP:0031908 Micrographia 0 SLC20A2 CL E G H 6575 10947 OMIM:213600 Basal ganglia calcification, idiopathic, 1 . 70 HP:0031908 HP:0031908 Micrographia 0 SNCA CL E G H 6622 11138 OMIM:168601 Parkinson disease 1, autosomal dominant . 65 HP:0031908 HP:0031908 Micrographia 0 SNCAIP CL E G H 9627 11139 OMIM:168600 Parkinson disease, late-onset . 35 HP:0031908 HP:0031908 Micrographia 0 TBP CL E G H 6908 11588 OMIM:168600 Parkinson disease, late-onset . 7 HP:0031908 HP:0031908 Micrographia 0 TRNT CL E G H 4576 7499 OMIM:168600 Parkinson disease, late-onset . HP:0031908 HP:0031908 Micrographia 0 VPS13A CL E G H 23230 1908 ORPHA:2388 Choreoacanthocytosis HP:0040283 - Occasional 130
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.