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46,XY Partial Gonadal Dysgenesis, with Minifascicular Neuropathy (DOID:9006824)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (0) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
46,XY sex reversal +     
polyneuropathy +     
46, XY Female 
46,Xy Gonadal Dysgenesis, Complete, Sry-Related  
46,XY Partial Gonadal Dysgenesis, with Minifascicular Neuropathy  
46,XY sex reversal 1  
46,XY sex reversal 10  
46,XY sex reversal 2  
46,XY sex reversal 3  
46,XY sex reversal 4  
46,XY sex reversal 5  
46,XY sex reversal 6  
46,XY sex reversal 7  
46,XY sex reversal 8  
46,XY sex reversal 9  
adult-onset ataxia and polyneuropathy  
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations 
alcoholic neuropathy  
Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia 
chronic polyneuropathy +  
congenital adrenal insufficiency  
demyelinating polyneuropathy +   
Genito Palato Cardiac Syndrome 
Gonadal Dysgenesis, Dysmorphic Facies, Retinal Dystrophy and Myopathy  
Gonadal Dysgenesis, XY Type, with Associated Anomalies 
gonadoblastoma +  
hereditary sensory neuropathy +   
idiopathic progressive polyneuropathy 
Kennerknecht Vogel Syndrome 
Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy 
Leukoencephalopathy with Dystonia and Motor Neuropathy  
Meacham Winn Culler Syndrome  
paraneoplastic polyneuropathy 
PCWH syndrome  
PHARC syndrome  
POEMS syndrome 
Polyendocrine-Polyneuropathy Syndrome  
polyneuropathy in collagen vascular disease 
polyradiculoneuropathy +   
Ribose 5-Phosphate Isomerase Deficiency  
Sensorineural Deafness with Peripheral Neuropathy and Arterial Disease 
sensory peripheral neuropathy  
Severe Infantile Axonal Neuropathy 
Spastic Paraplegia, Optic Atrophy, Microcephaly, and XY Sex Reversal 
Tangier disease  
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)  
Unilateral Aplasia of Extensor Muscles of Fingers, with Generalized Polyneuropathy 

Primary IDs: MESH:C567773
Alternate IDs: OMIM:607080 ;   RDO:0012039

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