Azoospermia

Symptom Information:

Symptom ID: HPO:0000027
Synonyms:
Azoospermia (disorder) [Orphanet:40720]
Infertility due to azoospermia (disorder) [Orphanet:40720]
Azoospermia (finding) [Orphanet:40720]
AZOSPERMIA [HPO:0000027]
Infertility due to azoospermia [Orphanet:40720]
Azoospermia [Orphanet:40720]
Azoospermia [OMIM:Azoospermia]
Azoospermia/oligospermia/asthenospermia [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: "Azoospermia" [OMIM:Azoospermia]
OMIM: "Oligozoospermia" [OMIM:Oligozoospermia]
OMIM: "Asthenospermia" [OMIM:Asthenospermia]
OMIM: "Asthenozoospermia (in some patients)" [OMIM:Asthenozoospermia (in some patients)]
UMLS:C0004509 "AZOSPERMIA" [HPO:0000027]
UMLS:C1321542 "Infertility due to azoospermia" [Orphanet:40720]
UMLS:C0004509 "Azoospermia" [Orphanet:40720]
UMLS:C0403823 "Asthenozoospermia" [Orphanet:40720]
Is a (Direct Parents):
Orphanet Infertility
MedDRA Spermatogenesis and semen disorders
HPO         Abnormal spermatogenesis
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)
                      Azoospermia(HPO:0000027)
MedDRA:
Reproductive system and breast disorders(MedDRA:10038604)
    Sexual function and fertility disorders(MedDRA:10013356)
       Spermatogenesis and semen disorders(MedDRA:10013358)
          Azoospermia(HPO:0000027)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

46,XX testicular disorder of sex development (Orphanet:393)
48,XXYY syndrome (Orphanet:10)
Bloom syndrome (Orphanet:125)
CILIARY DYSKINESIA, PRIMARY, 19 (OMIM:614935)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Congenital bilateral absence of vas deferens (Orphanet:48)
DELETED IN AZOOSPERMIA (OMIM:400003)
HYPOGONADISM WITH LOW-GRADE MENTAL DEFICIENCY AND MICROCEPHALY (OMIM:241000)
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA (OMIM:614897)
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA (OMIM:614837)
Hemochromatosis, type 1 (OMIM:235200)
Leukoencephalopathy - dystonia - motor neuropathy (Orphanet:163684)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
MURCS association (Orphanet:2578)
Male infertility due to NANOS1 mutation (Orphanet:352613)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
PREMATURE OVARIAN FAILURE 10 (OMIM:612885)
Partial androgen insensitivity syndrome (Orphanet:90797)
Renal cysts and diabetes syndrome (Orphanet:93111)
SPERMATOGENIC FAILURE 11 (OMIM:615081)
SPERMATOGENIC FAILURE 13 (OMIM:615841)
SPERMATOGENIC FAILURE 14 (OMIM:615842)
SPERMATOGENIC FAILURE 4 (OMIM:270960)
SPERMATOGENIC FAILURE 8 (OMIM:613957)
SPERMATOGENIC FAILURE, X-LINKED, 2 (OMIM:309120)
SPERMATOGENIC FAILURE, Y-LINKED, 2 (OMIM:415000)
Severe congenital hypochromic anemia with ringed sideroblasts (Orphanet:300298)
Young syndrome (Orphanet:3471)