Bifid scrotum
Symptom Information:
Symptom ID: | HPO:0000048 | |||||
Synonyms: |
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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: |
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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) |