Abnormality of the Leydig cells
Symptom Information:
Symptom ID: | HPO:0010789 | ||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal internal genitalia(HPO:0000812) Abnormality of male internal genitalia(HPO:0000022) Abnormality of the testis(HPO:0000035) Abnormality of the Leydig cells(HPO:0010789) Abnormality of the male genitalia(HPO:0010461) Abnormality of male internal genitalia(HPO:0000022) Abnormality of the testis(HPO:0000035) Abnormality of the Leydig cells(HPO:0010789) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
46,XY complete gonadal dysgenesis | (Orphanet:242) |