Hypometric saccades

Symptom Information:

Symptom ID: HPO:0000571
Synonyms:
Hypometric saccades [OMIM:Hypometric saccades]
Hypometric saccades (1 patient) [OMIM:Hypometric saccades (1 patient)]
Hypometric saccades (about half of patients) [OMIM:Hypometric saccades (about half of patients)]
Hypometric saccades (in some patients) [OMIM:Hypometric saccades (in some patients)]
Quality:
Cross references:
OMIM: "Hypometric saccades" [OMIM:Hypometric saccades]
OMIM: "Hypometric saccades (1 patient)" [OMIM:Hypometric saccades (1 patient)]
OMIM: "Hypometric saccades (about half of patients)" [OMIM:Hypometric saccades (about half of patients)]
OMIM: "Hypometric saccades (in some patients)" [OMIM:Hypometric saccades (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of saccadic eye movements
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of eye movement(HPO:0000496)
                Abnormality of saccadic eye movements(HPO:0000570)
                   Hypometric saccades(HPO:0000571)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Ataxia - oculomotor apraxia type 1 (Orphanet:1168)
Ataxia-telangiectasia-like disorder (Orphanet:251347)
Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome (Orphanet:363429)
Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency (Orphanet:324262)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Joubert syndrome 4 (OMIM:609583)
Joubert syndrome with renal defect (Orphanet:220497)
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency (Orphanet:352497)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Spectrin-associated autosomal recessive cerebellar ataxia (Orphanet:352403)