Infertility

Symptom Information:

Symptom ID: HPO:0000789
Synonyms:
Sterility [Orphanet:40630]
Sterility (finding) [Orphanet:40630]
Infertility [OMIM:Infertility]
Sterility/hypofertility [Orphanet:40630]
Infertility [MedDRA:10021926]
Infertility NOS [MedDRA:10021926]
Sterility [MedDRA:10021926]
Subfertility [MedDRA:10021926]
Fertility decreased [MedDRA:10021926]
Sterility post chemotherapy [MedDRA:10021926]
Infertility (in some male patients) [OMIM:Infertility (in some male patients)]
Infertility (in some patients) [OMIM:Infertility (in some patients)]
Subfertility [OMIM:Subfertility]
Quality:
Cross references:
Orphanet:40630 "Sterility/hypofertility" [Orphanet:40630]
OMIM: "Infertility" [OMIM:Infertility]
OMIM: "Infertility (in some male patients)" [OMIM:Infertility (in some male patients)]
OMIM: "Infertility (in some patients)" [OMIM:Infertility (in some patients)]
OMIM: "Subfertility" [OMIM:Subfertility]
UMLS:C0021359 "Infertility" [HPO:0000789]
UMLS:C0678108 "Sterility" [Orphanet:40630]
Is a (Direct Parents):
Orphanet Functional anomalies of the genital system
HPO         Decreased fertility
MedDRA Sexual function and fertility disorders NEC
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)
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)