Ambiguous genitalia, male
Symptom Information:
Symptom ID: | HPO:0000033 | ||||
Synonyms: |
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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 external genitalia(HPO:0000811) Abnormality of male external genitalia(HPO:0000032) Ambiguous genitalia, male(HPO:0000033) Ambiguous genitalia(HPO:0000062) Ambiguous genitalia, male(HPO:0000033) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Ambiguous genitalia, male(HPO:0000033) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG | (OMIM:218649) |
Denys-Drash syndrome | (Orphanet:220) |
Desmosterolosis | (Orphanet:35107) |
Exstrophy-epispadias complex | (Orphanet:322) |
Lathosterolosis | (Orphanet:46059) |
Meckel syndrome | (Orphanet:564) |
Pelviscapular dysplasia | (Orphanet:93333) |
Sudden infant death - dysgenesis of the testes | (Orphanet:168593) |