Female pseudohermaphroditism

Symptom Information:

Symptom ID: HPO:0010458
Synonyms:
Female pseudohermaphrodism [Orphanet:39080]
Female pseudohermaphroditism (disorder) [Orphanet:39080]
Female Pseudohermaphroditism [Orphanet:39080]
Female pseudohermaphrodism/virilisation/clitoridomegaly [Orphanet:39080]
Pseudohermaphroditism female [Orphanet:39080]
Pseudohermaphroditism female [MedDRA:10037123]
Female pseudohermaphroditism [MedDRA:10037123]
Quality:
Cross references:
Orphanet:39080 "Female pseudohermaphrodism/virilisation/clitoridomegaly" [Orphanet:39080]
UMLS:C0238394 "Female Pseudohermaphroditism" [Orphanet:39080]
Is a (Direct Parents):
Orphanet Ambiguous genitalia
MedDRA Female reproductive tract disorders congenital
HPO         Abnormality of female external genitalia
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 female genitalia(HPO:0010460)
                   Abnormality of female external genitalia(HPO:0000055)
                      Female pseudohermaphroditism(HPO:0010458)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of female external genitalia(HPO:0000055)
                      Female pseudohermaphroditism(HPO:0010458)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Reproductive tract and breast disorders congenital(MedDRA:10038608)
       Female reproductive tract disorders congenital(MedDRA:10016416)
          Female pseudohermaphroditism(HPO:0010458)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
46,XX disorder of sex development - skeletal anomalies (Orphanet:2975)
46,XY partial gonadal dysgenesis (Orphanet:251510)
Aromatase deficiency (Orphanet:91)
C syndrome (Orphanet:1308)
Congenital adrenal hyperplasia (Orphanet:418)
Ear-patella-short stature syndrome (Orphanet:2554)
Fraser syndrome (Orphanet:2052)
Hypertelorism, Teebi type (Orphanet:1519)
Leprechaunism (Orphanet:508)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
PAGOD syndrome (Orphanet:991)
Partial androgen insensitivity syndrome (Orphanet:90797)
Rabson-Mendenhall syndrome (Orphanet:769)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Zellweger syndrome (Orphanet:912)