Phenotypes for disease #03088 (CMH11 (cardiomyopathy, hypertrophic, familial, type 11 (CMH-11)), OMIM:612098)

15 entries on 1 page. Showing entries 1 - 15.
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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     
0000027221 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033819
0000027222 - - - Unknown - - - - - Johan den Dunnen 00033820
0000027223 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033821
0000027224 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00033822
0000027225 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033823
0000027226 - - - Unknown - - - - - Johan den Dunnen 00033824
0000027227 - - - Unknown - - - - - Johan den Dunnen 00033825
0000027228 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00033826
0000027229 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00033827
0000027235 - - - Unknown - - - - - Johan den Dunnen 00033833
0000027236 - - - Unknown - - - - - Johan den Dunnen 00033834
0000027240 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033838
0000027241 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033839
0000027242 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00033840
0000351722 Arthrogryposis multiplex congenita Distal amyotrophy Fatigable weakness Camptodactyly of 2nd-5th fingers Congenital myopathy - Isolated (sporadic) - - - - - Camille Verebi 00466358
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