Abnormality of the scrotum

Symptom Information:

Symptom ID: HPO:0000045
Synonyms:
Scrotum anomaly [Orphanet:39460]
Congenital abnormality of scrotum (disorder) [Orphanet:39460]
Disorder of scrotum (disorder) [Orphanet:39460]
Congenital abnormality of scrotum [Orphanet:39460]
Scrotum abnormalities [Orphanet:39460]
Scrotal disorder [Orphanet:39460]
Scrotal disorder [MedDRA:10062155]
Scrotal disorder NOS [MedDRA:10062155]
Scrotal induration [MedDRA:10062155]
Quality:
Cross references:
Orphanet:39460 "Scrotum abnormalities" [Orphanet:39460]
UMLS:C0341786 "Congenital abnormality of scrotum" [Orphanet:39460]
Is a (Direct Parents):
HPO         Abnormal scrotal rugation
HPO         Varicocele
HPO         Ectopic scrotum
HPO         Abnormality of male external genitalia
MedDRA Scrotal disorders NEC
HPO         Small scrotum
HPO         Scrotal hyperpigmentation
HPO         Scrotal pain
HPO         Accessory scrotum
Orphanet Structural anomalies of the genital system
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)
                      Abnormality of the scrotum(HPO:0000045)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the scrotum(HPO:0000045)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Penile and scrotal disorders (excl infections and inflammations)(MedDRA:10013355)
       Scrotal disorders NEC(MedDRA:10039745)
          Abnormality of the scrotum(HPO:0000045)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
46,XX ovotesticular disorder of sex development (Orphanet:2138)
Becker nevus syndrome (Orphanet:64755)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Distal monosomy 19p13.3 (Orphanet:96129)
GM1 gangliosidosis (Orphanet:354)
HEC syndrome (Orphanet:2119)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Infantile spasms - broad thumbs (Orphanet:3173)
Intellectual deficit, X-linked, Pai type (Orphanet:85322)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Postaxial polydactyly - dental and vertebral anomalies (Orphanet:2916)
Primary intestinal lymphangiectasia (Orphanet:90362)