Male pseudohermaphroditism
Symptom Information:
Symptom ID: | HPO:0000037 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
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) Abnormality of the male genitalia(HPO:0010461) Abnormality of male external genitalia(HPO:0000032) Male pseudohermaphroditism(HPO:0000037) Abnormal external genitalia(HPO:0000811) Abnormality of male external genitalia(HPO:0000032) Male pseudohermaphroditism(HPO:0000037) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Reproductive tract and breast disorders congenital(MedDRA:10038608) Male reproductive tract disorders congenital(MedDRA:10025517) Male pseudohermaphroditism(HPO:0000037) |
||||||||||
Database Frequency: | 25 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
46,XY SEX REVERSAL 1 | (OMIM:400044) |
46,XY complete gonadal dysgenesis | (Orphanet:242) |
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency | (Orphanet:752) |
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
46,XY disorder of sex development due to isolated 17, 20 lyase deficiency | (Orphanet:90796) |
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Androgen insensitivity syndrome | (Orphanet:754) |
Campomelic dysplasia | (Orphanet:140) |
Chondrodysplasia - disorder of sex development | (Orphanet:1422) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency | (Orphanet:90793) |
Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency | (Orphanet:90791) |
Currarino triad | (Orphanet:1552) |
Denys-Drash syndrome | (Orphanet:220) |
Disorder of sex development - intellectual deficit | (Orphanet:2983) |
Frasier syndrome | (Orphanet:347) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
LUTEINIZING HORMONE, BETA POLYPEPTIDE | (OMIM:152780) |
METHEMOGLOBINEMIA TYPE IV | (OMIM:250790) |
Meckel syndrome | (Orphanet:564) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Partial androgen insensitivity syndrome | (Orphanet:90797) |
Persistent Müllerian duct syndrome | (Orphanet:2856) |
Short rib-polydactyly syndrome | (Orphanet:1505) |
Testicular regression syndrome | (Orphanet:983) |