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Term:
congenital nystagmus 1 (DOID:0111790)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
46,XY sex reversal 2  
Abruzzo-Erickson syndrome  
Achromatopsia Incomplete, X-Linked 
Aicardi syndrome 
Aicardi-Goutieres syndrome +   
alpha-thalassemia myelodysplasia syndrome  
Alzheimer's disease 16 
AMME complex  
Amyotrophic Dystonic Paraplegia 
androgen insensitivity syndrome +   
Anencephaly and Spina Bifida X-Linked 
angioma serpiginosum +  
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction 
Arthrogryposis, X-Linked, Type V 
autosomal dominant disease +   
autosomal hemophilia A  
autosomal recessive congenital nystagmus 
autosomal recessive disease +   
blepharophimosis, ptosis, and epicanthus inversus syndrome +   
Bornholm Eye Disease 
Brachydactyly-Nystagmus-Cerebellar Ataxia 
Branchial Arch Syndrome X-Linked 
Bresheck/Bresek Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
cataract 40  
CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED  
Choroideremia +   
Chromosome Xq28 Duplication Syndrome 
Cleft Palate with Ankyloglossia  
combined T cell and B cell immunodeficiency +   
Cone Dystrophy, X-Linked, with Tapetal-like Sheen 
Congenital Adrenal Hypoplasia with Precocious Puberty 
Congenital Alopecia X-Linked 
congenital bilateral absence of vas deferens +   
Congenital Heart Defects, X-Linked +   
congenital hypogammaglobulinemia 
congenital nystagmus 1  
A congenital nystagmus that has_material_basis_in mutation in FRMD7 on chromosome Xq26.2. (DO)
congenital nystagmus 2 
congenital nystagmus 3 
congenital nystagmus 4 
congenital nystagmus 5 
congenital nystagmus 6  
congenital nystagmus 7 
Congenital Ptosis, Hereditary 2 
corpus callosum agenesis-abnormal genitalia syndrome  
Craniofacioskeletal Syndrome 
Deafness, High-Frequency Sensorineural, X-Linked 
deafness-intellectual disability, Martin-Probst type syndrome  
Dilated Cardiomyopathy 3A  
early infantile epileptic encephalopathy 8  
early infantile epileptic encephalopathy 9  
Epidermodysplasia Verruciformis, X-Linked 
Episodic Muscle Weakness, X-Linked 
External Ophthalmoplegia and Myopia 
exudative vitreoretinopathy 4  
Fabry disease +   
factor XI deficiency  
familial adenomatous polyposis +   
familial Mediterranean fever +   
favism  
Fetal Akinesia Syndrome, X-Linked 
Foveal Hypoplasia +   
Gillespie syndrome  
glycogen storage disease VIII 
Hodgkin Disease, X-Linked Pseudoautosomal 
Hydrocephalus with Cerebellar Agenesis 
Hypertrichosis Congenital Generalized X-Linked 
hypophosphatasia +   
Hypospadias 1, X-Linked  
Hypospadias 2, X-Linked  
Hypotonia, Congenital Nystagmus, Ataxia and Abnormal Auditory Brainstem Response 
Intracranial Berry Aneurysm 5 
Isolated Microphthalmia with Cataract 2  
Isolated Microphthalmia with Coloboma 1 
Isolated Noncompaction of the Ventricular Myocardium +   
Leigh Syndrome, X-Linked  
Macular Dystrophy, X-Linked +   
McCune Albright syndrome  
McLeod syndrome  
Meester-Loeys syndrome  
Melnick-Needles syndrome  
Membranoproliferative Glomerulonephritis, X-Linked 
Mental Retardation Mietens Weber Type 
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 
Mental Retardation, X-Linked +   
Microcephaly Microcornea Syndrome Seemanova Type 
Midline Defects, X-Linked 
Multiple Pterygium Syndrome, X-Linked 
Myopia 1 
Myopia 13 
Myopia 26, X-Linked, Female-Limited  
NEMO Mutation with Immunodeficiency 
Neural Tube Defects X-Linked 
Nystagmus 5, Infantile Periodic Alternating 
O'Donnell Pappas Syndrome  
Ogden syndrome  
optic atrophy 2 
ornithine carbamoyltransferase deficiency  
ovarian dysgenesis 2  
Parkinson's Disease 12 
Partial Agenesis of Corpus Callosum, X-Linked  
Periventricular Nodular Heterotopia 4  
Periventricular Nodular Heterotopia, with Frontometaphyseal Dysplasia 
Premature Ovarian Failure 2a  
progeria +   
Progressive Muscular Dystrophy, Pectorodorsal 
Prostate Cancer, Hereditary, X-Linked 1 
Prostate Cancer, Hereditary, X-Linked 2 
Radial Ray Deficiency, X-Linked 
Radiation Sensitivity of Natural Killer Activity 
Radius Absent Anogenital Anomalies 
reducing body myopathy 1B  
Reticuloendotheliosis, X-Linked 
retinitis pigmentosa 2  
retinitis pigmentosa 24 
retinitis pigmentosa 3  
retinitis pigmentosa 34 
retinitis pigmentosa 6  
retinitis pigmentosa 86  
Robinow syndrome +   
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked  
Russell-Silver Syndrome, X-Linked 
Selective Tooth Agenesis, X-Linked, 1  
septooptic dysplasia +   
Sketetal Dysplasia Coarse Facies Mental Retardation  
Sotos syndrome +   
SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY  
Spina Bifida, X-Linked 
split hand-foot malformation 2 
Spondylometaphyseal Dysplasia, X-Linked 
Surfactant Metabolism Dysfunction, Pulmonary, 4  
syndromic microphthalmia 12  
syndromic microphthalmia 13  
syndromic microphthalmia 14  
syndromic microphthalmia 8  
TARP syndrome  
terminal osseous dysplasia  
Testicular Germ Cell Tumor 1 
Thrombocythemia, X-Linked 
Thrombocytopenia 1  
thrombophilia due to thrombomodulin defect  
Thyroxine-Binding Globulin Deficiency +   
Torticollis Keloids Cryptorchidism Renal Dysplasia 
Vasquez Hurst Sotos Syndrome 
VEXAS syndrome  
Von Willebrand Disease, X-Linked Form 
Weill-Marchesani syndrome +   
Wells Jankovic Syndrome 
X Inactivation, Familial Skewed, 1  
X Inactivation, Familial Skewed, 2 
X-Linked Anemia with or without Neutropenia and/or Platelet Abnormalities  
X-Linked Anemia without Thrombocytopenia 
X-linked cardiac valvular dysplasia  
X-linked cleft palate with or without ankyloglossia  
X-linked cone-rod dystrophy 1  
X-linked cone-rod dystrophy 2 
X-linked congenital myopathy with fiber-type disproportion 
X-linked dilated cardiomyopathy  
X-linked dominant disease +   
X-linked epilepsy with variable learning disabilities and behavior disorders  
X-linked exudative vitreoretinopathy 2  
X-linked hereditary ataxia +   
X-Linked Hydrocephalus +   
X-Linked Hypogammaglobulinemia  
X-linked hypoparathyroidism 
X-Linked Immunodeficiency with Deficiency of 115,000 Dalton Surface Glycoprotein 
X-Linked Modifier for Neurofunctional Defects 
X-linked nonsyndromic deafness +   
X-linked panhypopituitarism  
X-linked recessive disease +   
X-linked reticulate pigmentary disorder  
X-linked retinitis pigmentosa and sinorespiratory infections  
X-linked Spondyloepimetaphyseal Dysplasia with Hypomyelinating Leukodystrophy   
X-Linked Tetra-Amelia 
X-Linked Thrombocytopenia, Intermittent  
X-Linked Thrombocytopenia, with or without Dyserythropoietic Anemia  
X-linked thrombophilia due to factor IX defect  
X-Linked Vesicoureteral Reflux 

Synonyms
Exact Synonyms: FRMD7-related infantile nystagmus ;   NYS1 ;   Nystagmus 1, Congenital, X- Linked ;   Nystagmus 1, Infantile, X-Linked ;   Nystagmus, congenital motor, 1 ;   X-Linked Congenital Nystagmus ;   X-linked idiopathic infantile nystagmus ;   X-linked infantile nystagmus ;   congenital motor nystagmus
Narrow Synonyms: IIN ;   NYSTAGMUS, INFANTILE IDIOPATHIC ;   NYSTAGMUS, INFANTILE PERIODIC ALTERNATING, X-LINKED ;   XIPAN ;   XLPAN
Primary IDs: MESH:C537853 ;   MESH:C580539
Alternate IDs: OMIM:310700
Xrefs: GARD:2969
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/17013395 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.