Male pseudohermaphroditism

Symptom Information:

Symptom ID: HPO:0000037
Synonyms:
Male pseudohermaphrodism [Orphanet:39060]
Male pseudohermaphroditism (disorder) [Orphanet:39060]
Male Pseudohermaphroditism [Orphanet:39060]
Male pseudohermaphroditism [OMIM:Male pseudohermaphroditism]
Male pseudohermaphrodism/lack of virilisation [Orphanet:39060]
Pseudohermaphroditism male [Orphanet:39060]
Pseudohermaphroditism male [MedDRA:10037124]
Male pseudohermaphroditism [MedDRA:10037124]
Partial androgen resistance [MedDRA:10037124]
Reifenstein's syndrome [MedDRA:10037124]
Quality:
Cross references:
Orphanet:39060 "Male pseudohermaphrodism/lack of virilisation" [Orphanet:39060]
OMIM: "Male pseudohermaphroditism" [OMIM:Male pseudohermaphroditism]
UMLS:C0238395 "Male Pseudohermaphroditism" [Orphanet:39060]
Is a (Direct Parents):
HPO         Abnormality of male external genitalia
Orphanet Ambiguous genitalia
MedDRA Male reproductive tract disorders congenital
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)
                      Male pseudohermaphroditism(HPO:0000037)
                Abnormality of the male genitalia(HPO:0010461)
                   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)