Infertility
Symptom Information:
Symptom ID: | HPO:0000789 | |||||||||||||
Synonyms: |
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Quality: | ||||||||||||||
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) Decreased fertility(HPO:0000144) Infertility(HPO:0000789) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Sexual function and fertility disorders(MedDRA:10013356) Sexual function and fertility disorders NEC(MedDRA:10013357) Infertility(HPO:0000789) |
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Database Frequency: | 74 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
3M syndrome | (Orphanet:2616) |
46,XX gonadal dysgenesis | (Orphanet:243) |
46,XX ovotesticular disorder of sex development | (Orphanet:2138) |
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency | (Orphanet:752) |
46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
ACTH-dependent Cushing syndrome | (Orphanet:99892) |
ACTH-independent Cushing syndrome | (Orphanet:99893) |
Alström syndrome | (Orphanet:64) |
Androgen insensitivity syndrome | (Orphanet:754) |
Aromatase deficiency | (Orphanet:91) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
Bloom syndrome | (Orphanet:125) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
CILIARY DYSKINESIA, PRIMARY, 13 | (OMIM:613193) |
CILIARY DYSKINESIA, PRIMARY, 14 | (OMIM:613807) |
CILIARY DYSKINESIA, PRIMARY, 15 | (OMIM:613808) |
CILIARY DYSKINESIA, PRIMARY, 2 | (OMIM:606763) |
CILIARY DYSKINESIA, PRIMARY, 22 | (OMIM:615444) |
CILIARY DYSKINESIA, PRIMARY, 24 | (OMIM:615481) |
CILIARY DYSKINESIA, PRIMARY, 25 | (OMIM:615482) |
CILIARY DYSKINESIA, PRIMARY, 26 | (OMIM:615500) |
CILIARY DYSKINESIA, PRIMARY, 29 | (OMIM:615872) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Classic galactosemia | (Orphanet:79239) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Cortisone reductase deficiency 1 | (OMIM:604931) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
Cystic fibrosis - gastritis - megaloblastic anemia | (Orphanet:2575) |
DEAFNESS, CATARACT, RETINITIS PIGMENTOSA, AND SPERM ABNORMALITIES | (OMIM:300719) |
Down syndrome | (Orphanet:870) |
Ectodermal dysplasia, Berlin type | (Orphanet:1816) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
FRAGILE SITE, DISTAMYCIN A TYPE, RARE, FRA(16)(q22.1) | (OMIM:136580) |
GLUCOCORTICOID RESISTANCE, GENERALIZED | (OMIM:615962) |
Globozoospermia | (Orphanet:171709) |
HYPERPROLACTINEMIA | (OMIM:615555) |
Hyperandrogenism due to cortisone reductase deficiency | (Orphanet:168588) |
Hypergonadotropic hypogonadism - cataract syndrome | (Orphanet:2410) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Isolated follicle stimulating hormone deficiency | (Orphanet:52901) |
Kallmann syndrome | (Orphanet:478) |
MORBID OBESITY AND SPERMATOGENIC FAILURE | (OMIM:615703) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Male infertility due to NANOS1 mutation | (Orphanet:352613) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Normosmic congenital hypogonadotropic hypogonadism | (Orphanet:432) |
OOCYTE MATURATION DEFECT | (OMIM:615774) |
Osteomesopyknosis | (Orphanet:2777) |
PROLACTIN DEFICIENCY, ISOLATED | (OMIM:264110) |
Partial androgen insensitivity syndrome | (Orphanet:90797) |
Prader-Willi syndrome | (Orphanet:739) |
Prune belly syndrome | (Orphanet:2970) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
SPERMATOGENIC FAILURE 1 | (OMIM:258150) |
SPERMATOGENIC FAILURE 10 | (OMIM:614822) |
SPERMATOGENIC FAILURE 11 | (OMIM:615081) |
SPERMATOGENIC FAILURE 6 | (OMIM:102530) |
Sneddon syndrome | (Orphanet:820) |
Testicular regression syndrome | (Orphanet:983) |
Testotoxicosis | (Orphanet:3000) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Usher syndrome | (Orphanet:886) |
Werner syndrome | (Orphanet:902) |
Xp22.3 microdeletion syndrome | (Orphanet:1643) |
Young syndrome | (Orphanet:3471) |