Background
Methods
Diseases
|
P value
a
|
---|---|
Infertility | <0.0001 |
Mutation abnormality | 0.0004 |
Malignant neoplasm of urinary organ, unspecified | 0.0010 |
Bladder neoplasm | 0.0010 |
Urologic neoplasms | 0.0010 |
Carcinoma of bladder | 0.0010 |
Neoplasm of unspecified nature of bladder | 0.0010 |
Urinary bladder diseases | 0.0011 |
B cell lymphomas | 0.0029 |
Liposarcoma, myxoid | 0.0036 |
Liposarcoma | 0.0037 |
Neoplasms, fibrous tissue | 0.0042 |
Juvenile dermatomyositis | 0.0044 |
Amyopathic dermatomyositis | 0.0044 |
Fibrosarcoma | 0.0044 |
Neoplasms, connective tissue | 0.0050 |
Liposarcoma, dedifferentiated | 0.0058 |
Frontotemporal lobar degeneration | 0.0074 |
Lymphoma, non Hodgkin | 0.0077 |
TDP 43 proteinopathies | 0.0098 |
Myositis | 0.0099 |
Diseases
|
P value
a
|
---|---|
Ovarian cysts | <0.0001 |
Gonadal dysgenesis | 0.0002 |
Leydig cell hypoplasia, type II | 0.0015 |
Donohue syndrome | 0.0015 |
Sulfocysteinuria | 0.0015 |
Primary hypogonadism | 0.0015 |
Diabetes mellitus, insulin resistant, with acanthosis nigricans | 0.0015 |
Sulfite oxidase deficiency | 0.0015 |
Ovarian hyperstimulation syndrome | 0.0015 |
Rabson Mendenhall syndrome | 0.0015 |
Eunuchism | 0.0030 |
Pseudohermaphroditism | 0.0030 |
ACTH deficiency, isolated | 0.0030 |
Isolated lutropin deficiency (disorder) | 0.0030 |
Lassa fever | 0.0031 |
Arenaviridae infections | 0.0031 |
Hemorrhagic fevers, viral | 0.0032 |
Precocious puberty | 0.0046 |
Liposarcoma, dedifferentiated | 0.0057 |
Gonadal dysgenesis, 46,XX | 0.0061 |
46, XX disorders of sex development | 0.0061 |
Synovial sarcoma | 0.0067 |
Multiple system congenital anomalies not elsewhere classified (NEC) in Systematized Nomenclature of Medicine Clinical Terms (SNOMED-CT) | 0.0076 |
Diseases
|
P value
a
|
---|---|
Hypergonadotropic ovarian failure, X linked | <0.0001 |
Premature menopause | <0.0001 |
Fragile X tremor/ataxia syndrome | <0.0001 |
POF7 (disorder) | <0.0001 |
Spermatogenic failure 8 | <0.0001 |
Hypoaldosteronism | <0.0001 |
Sex chromosome disorders | <0.0001 |
Adrenal cortical hypofunction | <0.0001 |
Fragile X syndrome | <0.0001 |
Adrenal gland hypofunction | 0.0001 |
Adrenal gland diseases | 0.0005 |
POF5 | 0.0008 |
POF6 | 0.0008 |
POF2b | 0.0008 |
Sex chromosome aberrations | 0.0008 |
Ptosis | 0.0016 |
Uterine prolapse without mention of vaginal wall prolapse | 0.0016 |
Eyelid diseases | 0.0024 |
Blepharophimosis | 0.0040 |
Blepharoptosis | 0.0071 |
Diseases
|
P value
a
|
---|---|
Female genital diseases | <0.0001 |
Uterine diseases | <0.0001 |
Myocardial infarction | <0.0001 |
Coronary artery disease | <0.0001 |
Sleep disorders, intrinsic | <0.0001 |
Parasomnia | <0.0001 |
Myocardial ischemia | <0.0001 |
Dementia due to specified medical condition | <0.0001 |
Restless legs syndrome | 0.0002 |
Diabetes mellitus, non-insulin dependent | 0.0005 |
Sex reversal, female, with dysgenesis of kidneys, adrenals, and lungs | 0.0016 |
46,XX testicular disorders of sex development | 0.0016 |
Disorder of pancreatic internal secretion | 0.0017 |
Hyperandrogenism | 0.0032 |
HIV infections | 0.0044 |
Carotid atherosclerosis | 0.0063 |
Pancreatic intraductal papillary mucinous adenoma | 0.0074 |
Aortic eneurysm, abdominal | 0.0095 |