Abnormality of the genital system
Symptom Information:
Symptom ID: | HPO:0000078 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) MedDRA: |
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Database Frequency: | 33 / 7739 | |||||||
Resource: |
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) |