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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
46,XY sex reversal 2  
Abruzzo-Erickson syndrome  
Achromatopsia Incomplete, X-Linked 
Aicardi syndrome  
alpha-thalassemia myelodysplasia syndrome  
Alzheimer's disease 16 
AMME complex 
androgen insensitivity syndrome +   
Anencephaly and Spina Bifida X-Linked 
angioma serpiginosum +  
Arthrogryposis, X-Linked, Type V 
Bornholm Eye Disease 
Branchial Arch Syndrome X-Linked 
Bresheck/Bresek Syndrome 
Bullous Dystrophy, Hereditary Macular Type 
cataract 40  
CEREBRAL-CEREBELLAR-COLOBOMA SYNDROME, X-LINKED  
Choroideremia +   
Chromosome Xq28 Duplication Syndrome  
Cleft Palate with Ankyloglossia  
combined T cell and B cell immunodeficiency +   
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  
Congenital Ptosis, Hereditary 2 
corpus callosum agenesis-abnormal genitalia syndrome  
Craniofacioskeletal Syndrome 
developmental and epileptic encephalopathy 90  
Dilated Cardiomyopathy 3A 
Epidermodysplasia Verruciformis, X-Linked 
Episodic Muscle Weakness, X-Linked 
External Ophthalmoplegia and Myopia 
Fabry disease +   
favism  
fetal akinesia deformation sequence syndrome X-linked 
High-Frequency Deafness, Sensorineural, X-Linked 
Hodgkin Disease, X-Linked Pseudoautosomal 
Hydrocephalus with Cerebellar Agenesis 
Hypertrichosis Congenital Generalized X-Linked 
Hypospadias 1, X-Linked  
Hypospadias 2, X-Linked  
intracranial berry aneurysm 5 
Isolated Noncompaction of the Ventricular Myocardium +   
Leigh Syndrome, X-Linked  
male infertility due to acephalic spermatozoa +   
male infertility due to globozoospermia +   
McLeod syndrome  
Meester-Loeys syndrome  
Melnick-Needles syndrome  
Membranoproliferative Glomerulonephritis, X-Linked 
Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 
Microcephaly Microcornea Syndrome Seemanova Type 
Microphthalmia/Coloboma 1 
Midline Defects, X-Linked 
Morbid Obesity and Spermatogenic Failure  
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 
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 
primary ovarian insufficiency 1  
Progressive Muscular Dystrophy, Pectorodorsal 
Prostate Cancer, Hereditary, X-Linked 1 
Prostate Cancer, Hereditary, X-Linked 2 
Pulmonary Surfactant Metabolism Dysfunction 4  
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  
ROLANDIC EPILEPSY, INTELLECTUAL DISABILITY, AND SPEECH DYSPRAXIA, X-LINKED  
Russell-Silver Syndrome, X-Linked 
Selective Tooth Agenesis, X-Linked, 1  
Sketetal Dysplasia Coarse Facies Mental Retardation  
spermatogenic failure 1  
spermatogenic failure 10  
spermatogenic failure 11  
spermatogenic failure 12  
spermatogenic failure 13  
spermatogenic failure 14  
spermatogenic failure 15  
spermatogenic failure 17  
spermatogenic failure 18  
spermatogenic failure 19  
spermatogenic failure 2  
spermatogenic failure 20  
spermatogenic failure 22  
spermatogenic failure 23  
spermatogenic failure 24  
spermatogenic failure 25  
spermatogenic failure 27  
spermatogenic failure 28  
spermatogenic failure 29  
spermatogenic failure 3  
spermatogenic failure 30  
spermatogenic failure 32  
spermatogenic failure 33  
spermatogenic failure 34  
spermatogenic failure 35  
spermatogenic failure 36  
spermatogenic failure 37  
spermatogenic failure 38  
spermatogenic failure 39  
spermatogenic failure 4  
spermatogenic failure 40  
spermatogenic failure 41  
spermatogenic failure 42  
spermatogenic failure 43  
spermatogenic failure 44  
spermatogenic failure 45  
spermatogenic failure 46  
spermatogenic failure 47  
spermatogenic failure 48  
spermatogenic failure 49  
spermatogenic failure 5  
spermatogenic failure 50  
spermatogenic failure 51  
spermatogenic failure 52  
spermatogenic failure 53  
spermatogenic failure 54  
spermatogenic failure 55  
spermatogenic failure 56  
spermatogenic failure 57  
spermatogenic failure 58  
spermatogenic failure 59  
spermatogenic failure 60  
spermatogenic failure 61  
spermatogenic failure 62  
spermatogenic failure 63  
spermatogenic failure 64  
spermatogenic failure 65  
Spermatogenic Failure 66  
Spermatogenic Failure 67  
Spermatogenic Failure 68  
Spermatogenic Failure 69  
spermatogenic failure 7  
Spermatogenic Failure 70  
Spermatogenic Failure 71  
Spermatogenic Failure 72  
Spermatogenic Failure 73  
Spermatogenic Failure 74  
Spermatogenic Failure 75  
Spermatogenic Failure 76  
Spermatogenic Failure 77  
Spermatogenic Failure 78  
Spermatogenic Failure 79  
spermatogenic failure 8  
Spermatogenic Failure 80  
Spermatogenic Failure 81  
Spermatogenic Failure 82  
Spermatogenic Failure 83  
Spermatogenic Failure 84  
Spermatogenic Failure 85  
Spermatogenic Failure 86  
Spermatogenic Failure 87  
Spermatogenic Failure 88  
Spermatogenic Failure 89  
Spermatogenic Failure 90  
Spina Bifida, X-Linked 
split hand-foot malformation 2 
Spondylometaphyseal Dysplasia, X-Linked 
syndromic microphthalmia 13  
Systemic Autoinflammatory Disease, X-Linked  
TARP syndrome  
terminal osseous dysplasia  
Testicular Germ Cell Tumor 1 
Thrombocythemia, X-Linked 
Thrombocytopenia 1  
Thyroxine-Binding Globulin Deficiency +   
Torticollis Keloids Cryptorchidism Renal Dysplasia 
Vasquez Hurst Sotos Syndrome 
VEXAS syndrome  
Von Willebrand Disease, X-Linked Form 
X Inactivation, Familial Skewed, 1  
X Inactivation, Familial Skewed, 2 
X-Linked Anemia without Thrombocytopenia 
X-linked cardiac valvular dysplasia  
X-linked central diabetes insipidus  
X-linked cleft palate with or without ankyloglossia  
X-Linked Cone Dystrophy with Tapetal-like Sheen 
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 2 with or without Impaired Intellectual Development and Dysmorphic Features  
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 Intellectual Developmental Disorders +   
X-Linked Macular Dystrophy +   
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 spermatogenic failure 2  
X-linked spermatogenic failure 3  
X-Linked Spermatogenic Failure 4  
X-Linked Spermatogenic Failure 5  
X-Linked Spermatogenic Failure 6  
X-Linked Spermatogenic Failure 7  
A male infertility due to significantly reduced sperm concentration and progressive motility, with abnormalities of the head and flagella. Caused by hemizygous mutation in the CT55 gene on chromosome Xq26.
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 Thrombophilia due to Factor VIII Defect  
X-Linked Vesicoureteral Reflux 
Y-linked spermatogenic failure 2  

Synonyms
Exact Synonyms: SPGFX7
Primary IDs: OMIM:301106
Definition Sources: OMIM:301106

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