Abnormality of the genital system

Symptom Information:

Symptom ID: HPO:0000078
Abnormality of the reproductive system [HPO:0000078]
Genital abnormalities [HPO:0000078]
Genital abnormality [HPO:0000078]
Genital anomalies [HPO:0000078]
Genital defects [HPO:0000078]
Genital anomalies [OMIM:Genital anomalies]
Genital defects [OMIM:Genital defects]
Cross references:
OMIM: "Genital anomalies" [OMIM:Genital anomalies]
OMIM: "Genital defects" [OMIM:Genital defects]
Is a (Direct Parents):
HPO         Abnormality of the genitourinary system
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the genital system(HPO:0000078)
Database Frequency: 33 / 7739

All diseases associated with this symptom:

6p22 microdeletion syndrome (Orphanet:251046)
6q25 microdeletion syndrome (Orphanet:251056)
ALG12-CDG (Orphanet:79324)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Aniridia (Orphanet:77)
Axial mesodermal dysplasia spectrum (Orphanet:1834)
Bartsocas-Papas syndrome (Orphanet:1234)
Blackfan-Diamond anemia (Orphanet:124)
Cat-eye syndrome (Orphanet:195)
Caudal duplication (Orphanet:1756)
Cystinosis (Orphanet:213)
Hemochromatosis type 2 (Orphanet:79230)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Insulin-resistance syndrome type A (Orphanet:2297)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
MELAS (Orphanet:550)
Mitochondrial myopathy and sideroblastic anemia (Orphanet:2598)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Orofaciodigital syndrome type 2 (Orphanet:2751)
PAGOD syndrome (Orphanet:991)
Penoscrotal transposition (Orphanet:2842)
Renal cysts and diabetes syndrome (Orphanet:93111)
Short rib-polydactyly syndrome (Orphanet:1505)
Sirenomelia (Orphanet:3169)
Urban-Rogers-Meyer syndrome (Orphanet:3409)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wolfram syndrome (Orphanet:3463)
Woodhouse-Sakati syndrome (Orphanet:3464)
Young syndrome (Orphanet:3471)