Abnormal spermatogenesis

Symptom Information:

Symptom ID: HPO:0008669
Synonyms:
Abnormal sperm development [HPO:0008669]
Impaired spermatogenesis [HPO:0008669]
Impaired spermatogenesis [OMIM:Impaired spermatogenesis]
Spermatogenesis abnormal [MedDRA:10041493]
Quality:
Cross references:
OMIM: "Impaired spermatogenesis" [OMIM:Impaired spermatogenesis]
Is a (Direct Parents):
MedDRA Spermatogenesis and semen disorders
HPO         Functional abnormality of male internal genitalia
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)
             Abnormality of reproductive system physiology(HPO:0000080)
                Functional abnormality of male internal genitalia(HPO:0000025)
                   Abnormal spermatogenesis(HPO:0008669)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Sexual function and fertility disorders(MedDRA:10013356)
       Spermatogenesis and semen disorders(MedDRA:10013358)
          Abnormal spermatogenesis(HPO:0008669)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

48,XXXY syndrome (Orphanet:96263)
49,XXXXY syndrome (Orphanet:96264)
8p11.2 deletion syndrome (Orphanet:251066)
ATAXIA-TELANGIECTASIA (OMIM:208900)
Alström syndrome (Orphanet:64)
Ataxia-telangiectasia (Orphanet:100)
Deafness-infertility syndrome (Orphanet:94064)
Fanconi anemia (Orphanet:84)
Oculocerebrorenal syndrome (Orphanet:534)
Testotoxicosis (Orphanet:3000)
Williams syndrome (Orphanet:904)