Chordee

Symptom Information:

Symptom ID: HPO:0000041
Synonyms:
Angulation of penis [Orphanet:39280]
Deformity of erection (disorder) [Orphanet:39280]
Penis bent (finding) [Orphanet:39280]
Penis bent [Orphanet:39280]
Deformity of erection [Orphanet:39280]
Chordee [OMIM:Chordee]
Hypospadias/epispadias/bent penis [Orphanet:39280]
Chordee [MedDRA:10008746]
Quality:
Cross references:
Orphanet:39280 "Hypospadias/epispadias/bent penis" [Orphanet:39280]
OMIM: "Chordee" [OMIM:Chordee]
UMLS:C0221182 "Chordee" [HPO:0000041]
UMLS:C0403769 "Penis bent" [Orphanet:39280]
UMLS:C0549144 "Deformity of erection" [Orphanet:39280]
Is a (Direct Parents):
Orphanet Epispadias
Orphanet Abnormality of the penis
HPO         Abnormality of the penis
MedDRA Male reproductive tract disorders congenital
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 penis(HPO:0000036)
                         Chordee(HPO:0000041)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Abnormality of the penis(HPO:0000036)
                         Chordee(HPO:0000041)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Reproductive tract and breast disorders congenital(MedDRA:10038608)
       Male reproductive tract disorders congenital(MedDRA:10025517)
          Chordee(HPO:0000041)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

46,XY SEX REVERSAL 6 (OMIM:613762)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
Cryptomicrotia - brachydactyly - excess fingertip arch (Orphanet:1547)
Hand-foot-genital syndrome (Orphanet:2438)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
MICROPHTHALMIA, SYNDROMIC 7 (OMIM:309801)
Marden-Walker syndrome (Orphanet:2461)
Mowat-Wilson syndrome (Orphanet:2152)
Osteoglophonic dwarfism (Orphanet:2645)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Renal cysts and diabetes syndrome (Orphanet:93111)