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Ontology Browser

autosomal hemophilia A (DOID:0111823)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Aicardi-Goutieres syndrome +   
autosomal dominant disease +   
autosomal hemophilia A  
A blood coagulation disease characterized by autosomal inheritence of a Factor VIII deficiency. (DO)
autosomal recessive disease +   
blepharophimosis, ptosis, and epicanthus inversus syndrome  
camptodactyly-tall stature-scoliosis-hearing loss syndrome  
congenital nystagmus 1  
exudative vitreoretinopathy 4  
Factor V and Factor VIII, Combined Deficiency of, 2  
Factor VIII Deficiency, Acquired  
factor XI deficiency  
familial adenomatous polyposis +   
familial Mediterranean fever +   
Familial Multiple Coagulation Factor Deficiency I  
Gillespie syndrome  
Hemophilia A with Vascular Abnormality 
hypophosphatasia +   
McCune Albright syndrome  
progeria +   
Robinow syndrome +   
septooptic dysplasia +   
syndromic microphthalmia 12  
syndromic microphthalmia 14  
syndromic microphthalmia 8  
thrombophilia due to thrombomodulin defect  
Weill-Marchesani syndrome +   

Exact Synonyms: autosomal factor VIII deficiency
Narrow Synonyms: MILD HEMOPHILIA A
Primary IDs: OMIM:134500
Definition Sources: "DO"

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