Oligospermia
Symptom Information:
Symptom ID: | HPO:0000798 | |||||||||||||||||||
Synonyms: |
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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) Abnormality of reproductive system physiology(HPO:0000080) Functional abnormality of male internal genitalia(HPO:0000025) Abnormal spermatogenesis(HPO:0008669) Oligospermia(HPO:0000798) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Sexual function and fertility disorders(MedDRA:10013356) Spermatogenesis and semen disorders(MedDRA:10013358) Oligospermia(HPO:0000798) |
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Database Frequency: | 13 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Alström syndrome | (Orphanet:64) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
CATSPER1-related non syndromic male infertility | (Orphanet:276234) |
CILIARY DYSKINESIA, PRIMARY, 19 | (OMIM:614935) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Fabry disease | (Orphanet:324) |
MORBID OBESITY AND SPERMATOGENIC FAILURE | (OMIM:615703) |
Proximal myotonic myopathy | (Orphanet:606) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
SPERMATOGENIC FAILURE 11 | (OMIM:615081) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |