Phenotypes for disease #04302 (FANCS (Fanconi anemia, complementation group S (FANCS)))

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000054418 hypertelorism, epicanthal folds, ptosis, strabismus, blepharophimosis, broad nasal bridge and nasal tip, and proximally inserted thumbs - - Familial, autosomal recessive - - - - - Arleen D. Auerbach 00074676
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