Phenotypes for disease #04242 (FRDA (Friedreich ataxia (FRDA)), OMIM:229300)

17 entries on 1 page. Showing entries 1 - 17.
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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     
0000028249 8596916-Fam1 - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037733
0000028250 8596916-Fam2 - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037734
0000028251 8596916-Fam3a - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037735
0000028252 8596917-Fam3b - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037736
0000028253 8596918-Fam3c - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037737
0000028255 08596916-dis - - Familial - - - - - Johan den Dunnen 00037739
0000028256 ? - - Isolated (sporadic) 24y - - - - Nazli Basak 00037740
0000028257 08596916-Fam4 - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037741
0000028258 08596916-Fam5 - - Familial, autosomal recessive - - - - - Johan den Dunnen 00037742
0000034304 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00046847
0000046786 Friedreich ataxia-like, see paper; ..., - - Familial, autosomal recessive - - - - - Johan den Dunnen 00060288
0000299877 - Friedreich ataxia - Familial, autosomal recessive - - - - - Johan den Dunnen 00407742
0000299878 - Friedreich ataxia - Familial, autosomal recessive - - - - - Johan den Dunnen 00407743
0000299879 - Friedreich ataxia - Familial, autosomal recessive - - - - - Johan den Dunnen 00407744
0000299929 3t-ataxia, 4y-severe cardiomyopathy Friedreich's ataxia FRDA Familial, autosomal recessive - - - - - Johan den Dunnen 00407801
0000299930 ataxia, scoliosis, 27y-wheelchair-bound, slow progression, signs of cardiac hypertrophy and dysarthria Friedreich's ataxia FRDA Familial, autosomal recessive - - - - - Johan den Dunnen 00407800
0000299931 ataxia, foot deformity, scoliosis, axonal sensory neuropathy, mild dysarthria, 15y-wheelchairbound, 21y-hypertrophic cardiomyopathy, atrophy cervical spinal cord and upper cerebellar vermis Friedreich's ataxia FRDA Familial, autosomal recessive - - - - - Johan den Dunnen 00407799
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