Oligospermia

Symptom Information:

Symptom ID: HPO:0000798
Synonyms:
Infertility due to oligospermia (disorder) [Orphanet:40720]
Infertility due to oligospermia [Orphanet:40720]
Oligospermia [Orphanet:40720]
Oligospermia [OMIM:Oligospermia]
Azoospermia/oligospermia/asthenospermia [Orphanet:40720]
Oligozoospermia [Orphanet:40720]
Azoospermia [MedDRA:10003883]
Azospermia [MedDRA:10003883]
Oligospermia [MedDRA:10003883]
Oligozoospermia [MedDRA:10003883]
Spermatogenesis arrest [MedDRA:10003883]
Spermatogenesis arrested [MedDRA:10003883]
Spermatogenesis reversible inhibition of [MedDRA:10003883]
Oligozoospermia [OMIM:Oligozoospermia]
Asthenospermia [MedDRA:10067162]
Asthenozoospermia (finding) [Orphanet:40720]
Asthenozoospermia [Orphanet:40720]
Asthenospermia [OMIM:Asthenospermia]
Asthenozoospermia (in some patients) [OMIM:Asthenozoospermia (in some patients)]
Quality:
Cross references:
Orphanet:40720 "Azoospermia/oligospermia/asthenospermia" [Orphanet:40720]
OMIM: "Oligospermia" [OMIM:Oligospermia]
OMIM: "Oligozoospermia" [OMIM:Oligozoospermia]
OMIM: "Asthenospermia" [OMIM:Asthenospermia]
OMIM: "Asthenozoospermia (in some patients)" [OMIM:Asthenozoospermia (in some patients)]
UMLS:C0868910 "Oligospermia" [HPO:0000798]
UMLS:C0268980 "Infertility due to oligospermia" [Orphanet:40720]
UMLS:C0028960 "Oligospermia" [Orphanet:40720]
UMLS:C0403823 "Asthenozoospermia" [Orphanet:40720]
Is a (Direct Parents):
MedDRA Spermatogenesis and semen disorders
HPO         Abnormal spermatogenesis
Orphanet Azoospermia
Orphanet Infertility
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)
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)