Human Phenotype Ontology 
Grandparent Node:
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Abnormal involuntary eye movements (HP:0012547)help
Parent Node:
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Nystagmus (HP:0000639)help
..Starting node
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Nystagmus-induced head nodding (HP:0001361)help
Term ID: 1361
Name: Nystagmus-induced head nodding
Synonym:
Definition: Head movements associated with nystagmus, that may represent an attempt to compensate for the involuntary eye movements and to improve vision.
Comments:
Reference: HP:0001361
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCongenital nystagmus (HP:0006934) help
..expandDivergence nystagmus (HP:0030691) help
..expandGaze-evoked nystagmus (HP:0000640) help
..expandHorizontal nystagmus (HP:0000666) help
..expandPendular nystagmus (HP:0012043) help
..expandRotary nystagmus (HP:0001583) help
..expandVertical nystagmus (HP:0010544) help
..expandVestibular nystagmus (HP:0010542) 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:0001361HP:0001361Nystagmus-induced head nodding0BAZ1B CL E G H9031961ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0BCL7B CL E G H92751005ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0BUD23 CL E G H11404916405ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0CLIP2 CL E G H74612586ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0DNAJC30 CL E G H8427716410ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0EIF4H CL E G H745812741ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0ELN CL E G H20063327ORPHA:904Williams syndromeHP:0040282 - Frequent172
HP:0001361HP:0001361Nystagmus-induced head nodding0FKBP6 CL E G H84683722ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0GPR143 CL E G H493520145OMIM:300500Albinism, ocular, type I.64
HP:0001361HP:0001361Nystagmus-induced head nodding0GTF2I CL E G H29694659ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0001361HP:0001361Nystagmus-induced head nodding0GTF2IRD1 CL E G H95694661ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0001361HP:0001361Nystagmus-induced head nodding0GTF2IRD2 CL E G H8416330775ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0001361HP:0001361Nystagmus-induced head nodding0LIMK1 CL E G H39846613ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0METTL27 CL E G H15536819068ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0001361HP:0001361Nystagmus-induced head nodding0MLXIPL CL E G H5108512744ORPHA:904Williams syndromeHP:0040282 - Frequent1
HP:0001361HP:0001361Nystagmus-induced head nodding0NCF1 CL E G H6533617660ORPHA:904Williams syndromeHP:0040282 - Frequent13
HP:0001361HP:0001361Nystagmus-induced head nodding0RFC2 CL E G H59829970ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0STX1A CL E G H680411433ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0TBL2 CL E G H2660811586ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0TMEM270 CL E G H13588623018ORPHA:904Williams syndromeHP:0040282 - Frequent
HP:0001361HP:0001361Nystagmus-induced head nodding0VPS37D CL E G H15538218287ORPHA:904Williams syndromeHP:0040282 - Frequent


Genes (21) :BAZ1B BCL7B BUD23 CLIP2 DNAJC30 EIF4H ELN FKBP6 GPR143 GTF2I GTF2IRD1 GTF2IRD2 LIMK1 METTL27 MLXIPL NCF1 RFC2 STX1A TBL2 TMEM270 VPS37D

Diseases (2) :ORPHA:904 OMIM:300500
 

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