Human Phenotype Ontology 
Grandparent Node:
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Abnormality of coordination (HP:0011443)help
Parent Node:
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Incoordination (HP:0002311)help
..Starting node
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Poor coordination (HP:0002370)help
Term ID: 2370
Name: Poor coordination
Synonym: Poor coordination
Definition:
Comments:
Reference: HP:0002370
Genes and Diseases:
 
       Child Nodes:
........expandPoor hand-eye coordination (HP:0007057) help

 Sister Nodes: 
..expandClumsiness (HP:0002312) help
..expandFrequent falls (HP:0002359) 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:0002370HP:0002370Poor coordination0AFF2 CL E G H23343776OMIM:309548Mental retardation, X-linked, associated with fragile site fraxe59
HP:0002370HP:0002370Poor coordination0APC2 CL E G H1029724036ORPHA:821Sotos syndromeHP:0040283 - Occasional1
HP:0002370HP:0002370Poor coordination0ARL6 CL E G H8410013210OMIM:209900Bardet-Biedl syndrome 1.29
HP:0002370HP:0002370Poor coordination0BBS1 CL E G H582966OMIM:209900Bardet-Biedl syndrome 1.114
HP:0002370HP:0002370Poor coordination0CARS1 CL E G H8331493OMIM:618891MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME; MDBH
HP:0002370HP:0002370Poor coordination0CCDC28B CL E G H7914028163OMIM:209900Bardet-Biedl syndrome 1.4
HP:0002370HP:0002370Poor coordination0CDC42BPB CL E G H95781738OMIM:619841
HP:0002370HP:0002370Poor coordination0CREBBP CL E G H13872348OMIM:180849Rubinstein-Taybi syndrome 1291
HP:0002370HP:0002370Poor coordination0EED CL E G H87263188OMIM:617561Cohen-Gibson syndrome.4
HP:0002370HP:0002370Poor coordination0ELN CL E G H20063327OMIM:194050Williams-Beuren syndrome.172
HP:0002370HP:0002370Poor coordination0EP300 CL E G H20333373OMIM:180849Rubinstein-Taybi syndrome 1250
HP:0002370HP:0002370Poor coordination0ERCC4 CL E G H20723436OMIM:610965XFE progeroid syndrome.158
HP:0002370HP:0002370Poor coordination0HSD17B10 CL E G H30284800ORPHA:391428HSD10 disease, infantile typeHP:0040283 - Occasional19
HP:0002370HP:0002370Poor coordination0HUWE1 CL E G H1007530892OMIM:309590Mental retardation, x-linked syndromic, Turner type.98
HP:0002370HP:0002370Poor coordination0KCNA1 CL E G H37366218ORPHA:37612Episodic ataxia type 1HP:0040281 - Very frequent145
HP:0002370HP:0002370Poor coordination0KCND3 CL E G H37526239ORPHA:98772Spinocerebellar ataxia type 19/22HP:0040283 - Occasional35
HP:0002370HP:0002370Poor coordination0LZTFL1 CL E G H545856741OMIM:615994BARDET-BIEDL SYNDROME 17; BBS174
HP:0002370HP:0002370Poor coordination0MLXIPL CL E G H5108512744OMIM:194050Williams-Beuren syndrome.1
HP:0002370HP:0002370Poor coordination0MTR CL E G H45487468OMIM:250940Homocystinuria-megaloblastic anemia, cblg Complementation type.217
HP:0002370HP:0002370Poor coordination0NAA20 CL E G H5112615908OMIM:619717INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 73; MRT73
HP:0002370HP:0002370Poor coordination0NIPA1 CL E G H12360617043ORPHA:26118315q11.2 microdeletion syndromeHP:0040283 - Occasional117
HP:0002370HP:0002370Poor coordination0NIPA2 CL E G H8161417044ORPHA:26118315q11.2 microdeletion syndromeHP:0040283 - Occasional1
HP:0002370HP:0002370Poor coordination0NSD1 CL E G H6432414234ORPHA:821Sotos syndromeHP:0040283 - Occasional544
HP:0002370HP:0002370Poor coordination0NSD1 CL E G H6432414234OMIM:117550Sotos syndrome 1544
HP:0002370HP:0002370Poor coordination0PDE2A CL E G H51388777OMIM:619150INTELLECTUAL DEVELOPMENTAL DISORDER WITH PAROXYSMAL DYSKINESIA OR SEIZURES; IDDPADS
HP:0002370HP:0002370Poor coordination0RNF168 CL E G H16591826661ORPHA:420741RIDDLE syndrome7
HP:0002370HP:0002370Poor coordination0SETD2 CL E G H2907218420ORPHA:821Sotos syndromeHP:0040283 - Occasional60
HP:0002370HP:0002370Poor coordination0SIM1 CL E G H649210882ORPHA:1718296q16 microdeletion syndromeHP:0040283 - Occasional40
HP:0002370HP:0002370Poor coordination0SLC25A15 CL E G H1016610985ORPHA:415Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeHP:0040282 - Frequent88
HP:0002370HP:0002370Poor coordination0SLC25A15 CL E G H1016610985OMIM:238970Hyperornithinemia-Hyperammonemia-Homocitrullinuria syndrome.88
HP:0002370HP:0002370Poor coordination0SLC6A8 CL E G H653511055OMIM:300352Creatine deficiency syndrome, X-linked122
HP:0002370HP:0002370Poor coordination0SYNGAP1 CL E G H883111497ORPHA:544254SYNGAP1-related developmental and epileptic encephalopathyHP:0040282 - Frequent108
HP:0002370HP:0002370Poor coordination0TANGO2 CL E G H12898925439OMIM:616878Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration12
HP:0002370HP:0002370Poor coordination0TBC1D23 CL E G H5577325622OMIM:617695Pontocerebellar hypoplasia, type 11.
HP:0002370HP:0002370Poor coordination0TCF20 CL E G H694211631OMIM:618430Developmental delay with variable intellectual impairment and behavioral abnormalities.1
HP:0002370HP:0002370Poor coordination0TUBG1 CL E G H728312417ORPHA:26118315q11.2 microdeletion syndromeHP:0040283 - Occasional14
HP:0002370HP:0002370Poor coordination0TXN2 CL E G H2582817772ORPHA:478029Combined oxidative phosphorylation defect type 29HP:0040281 - Very frequent1
HP:0002370HP:0002370Poor coordination0YWHAG CL E G H753212852OMIM:617665Epileptic encephalopathy, early infantile, 56.
HP:0002370HP:0007057Poor hand-eye coordination1RNF168 CL E G H16591826661ORPHA:420741RIDDLE syndromeHP:0040283 - Occasional7
HP:0002370HP:0007057Poor hand-eye coordination1SLC6A8 CL E G H653511055OMIM:300352Creatine deficiency syndrome, X-linked.122


Genes (36) :AFF2 APC2 ARL6 BBS1 CARS1 CCDC28B CDC42BPB CREBBP EED ELN EP300 ERCC4 HSD17B10 HUWE1 KCNA1 KCND3 LZTFL1 MLXIPL MTR NAA20 NIPA1 NIPA2 NSD1 PDE2A RNF168 SETD2 SIM1 SLC25A15 SLC6A8 SYNGAP1 TANGO2 TBC1D23 TCF20 TUBG1 TXN2 YWHAG

Diseases (30) :OMIM:309548 ORPHA:821 OMIM:209900 OMIM:618891 OMIM:619841 OMIM:180849 OMIM:617561 OMIM:194050 OMIM:610965 ORPHA:391428 OMIM:309590 ORPHA:37612 ORPHA:98772 OMIM:615994 OMIM:250940 OMIM:619717 ORPHA:261183 OMIM:117550 OMIM:619150 ORPHA:420741 ORPHA:171829 ORPHA:415 OMIM:238970 OMIM:300352 ORPHA:544254 OMIM:616878 OMIM:617695 OMIM:618430 ORPHA:478029 OMIM:617665
 

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