Congenital macroorchidism

Symptom Information:

Symptom ID: HPO:0008640
Synonyms:
Congenital macroorchidism (in some patients) [OMIM:Congenital macroorchidism (in some patients)]
Quality:
Cross references:
OMIM: "Congenital macroorchidism (in some patients)" [OMIM:Congenital macroorchidism (in some patients)]
Is a (Direct Parents):
HPO         Macroorchidism
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)
                         Macroorchidism(HPO:0000053)
                            Congenital macroorchidism(HPO:0008640)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male internal genitalia(HPO:0000022)
                      Abnormality of the testis(HPO:0000035)
                         Macroorchidism(HPO:0000053)
                            Congenital macroorchidism(HPO:0008640)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Fragile X syndrome (Orphanet:908)