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 entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0001361HP:0001361Nystagmus-induced head nodding0BAZ1B CL E G H9031904Blepharophimosis nasal groove growth retardationORPHA15961605681
HP:0001361HP:0001361Nystagmus-induced head nodding0CLIP2 CL E G H7461904Blepharophimosis nasal groove growth retardationORPHA112586603432
HP:0001361HP:0001361Nystagmus-induced head nodding0ELN CL E G H2006904Blepharophimosis nasal groove growth retardationORPHA11273327130160
HP:0001361HP:0001361Nystagmus-induced head nodding0GPR143 CL E G H4935300500Ocular albinism, type I300500C0342684OMIM118120145300808
HP:0001361HP:0001361Nystagmus-induced head nodding0GTF2I CL E G H2969904Blepharophimosis nasal groove growth retardationORPHA114659601679
HP:0001361HP:0001361Nystagmus-induced head nodding0GTF2IRD1 CL E G H9569904Blepharophimosis nasal groove growth retardationORPHA164661604318
HP:0001361HP:0001361Nystagmus-induced head nodding0LIMK1 CL E G H3984904Blepharophimosis nasal groove growth retardationORPHA176613601329
HP:0001361HP:0001361Nystagmus-induced head nodding0RFC2 CL E G H5982904Blepharophimosis nasal groove growth retardationORPHA149970600404
HP:0001361HP:0001361Nystagmus-induced head nodding0TBL2 CL E G H26608904Blepharophimosis nasal groove growth retardationORPHA111586605842
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (9) :BAZ1B CLIP2 ELN GPR143 GTF2I GTF2IRD1 LIMK1 RFC2 TBL2

Diseases (2) :904 300500
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.