Azoospermia
Symptom Information:
Symptom ID: | HPO:0000027 | |||||||||||||||||||||
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) 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) |
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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) |