Bifid scrotum

Symptom Information:

Symptom ID: HPO:0000048
Synonyms:
Bifid scrotum (disorder) [Orphanet:39540]
Bifid scrotum [Orphanet:39540]
Bifid scrotum [OMIM:Bifid scrotum]
Bifid scrotum (in 1 of 3 siblings) [OMIM:Bifid scrotum (in 1 of 3 siblings)]
Bifid scrotum (in 1 of 6 patients) [OMIM:Bifid scrotum (in 1 of 6 patients)]
Quality:
Cross references:
Orphanet:39540 "Bifid scrotum" [Orphanet:39540]
OMIM: "Bifid scrotum" [OMIM:Bifid scrotum]
OMIM: "Bifid scrotum (in 1 of 3 siblings)" [OMIM:Bifid scrotum (in 1 of 3 siblings)]
OMIM: "Bifid scrotum (in 1 of 6 patients)" [OMIM:Bifid scrotum (in 1 of 6 patients)]
UMLS:C0341787 "Bifid scrotum" [Orphanet:39540]
Is a (Direct Parents):
Orphanet Abnormality of the scrotum
HPO         Abnormality of the scrotum
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)
                      Abnormality of the scrotum(HPO:0000045)
                         Bifid scrotum(HPO:0000048)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the scrotum(HPO:0000045)
                         Bifid scrotum(HPO:0000048)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
3MC SYNDROME 3 (OMIM:248340)
46,XX ovotesticular disorder of sex development (Orphanet:2138)
46,XX testicular disorder of sex development (Orphanet:393)
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency (Orphanet:753)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Beta-ureidopropionase deficiency (Orphanet:65287)
Brachytelephalangy - dysmorphism - Kallmann syndrome (Orphanet:1295)
CHARGE syndrome (Orphanet:138)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Craniofacial-ulnar-renal syndrome (Orphanet:293843)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Currarino triad (Orphanet:1552)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Fetal hydantoin syndrome (Orphanet:1912)
Fryns syndrome (Orphanet:2059)
Hand-foot-genital syndrome (Orphanet:2438)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
MELAS (Orphanet:550)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mowat-Wilson syndrome (Orphanet:2152)
Opitz G/BBB syndrome (Orphanet:2745)
PELVIS syndrome (Orphanet:83628)
Partial androgen insensitivity syndrome (Orphanet:90797)
Penoscrotal transposition (Orphanet:2842)
SCARF syndrome (Orphanet:3134)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Townes-Brocks syndrome (Orphanet:857)
VACTERL/VATER association (Orphanet:887)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)