Phenotypes for disease #00161 (CHARGE (CHARGE Syndrome), OMIM:214800)

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AscendingPhenotype ID     

Phenotype details     

Inheritance     

Owner     

Individual ID     
0000000312 constitutional delay in growth and puberty, she was pre-pubertal with no breast, axillary hair or pubic hair development, a CT scan of the temporal bones showed absence of all the semicircular canals bilaterally - Nur Aisyah Athirah 00000797
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