User:Keilana/Worklist

OB/GYN

 * Bimanual examination (needs a separate article)
 * Breast examination (needs a separate article)
 * Saline infusion sonography
 * Tuboovarian infection/tuboovarian complex/tuboovarian abscess
 * Voiding cystourethrography
 * Positive pressure urethrography
 * Selective salpingography
 * Suppurative cervicitis
 * Vaginal cuff cellulitis
 * Pelvic cellulitis
 * Ovarian abscess
 * Pelvic abscess
 * Vulvar abscess
 * Bartholin gland duct abscess
 * Skene gland cyst
 * Urethral diverticulum
 * Vulvovaginal trauma
 * Straddle injury
 * Vaginal foreign body
 * Desquamative inflammatory vaginitis
 * Cervical eversion
 * Endocervical polyp
 * Intrauterine contraception - redirect to intrauterine device when off mobile
 * Progestin implant - redirect to contraceptive implant
 * Transcervical sterilization
 * Aneuploid abortion
 * Threatened abortion/Threatened miscarriage
 * Inevitable abortion/Inevitable miscarriage
 * Missed abortion (early pregnancy loss)
 * Luteal phase defect
 * Salpingostomy
 * Caesarian scar pregnancy
 * Withdrawal bleeding
 * Mullerian defect
 * Ovarian cystectomy
 * pseudo-Meigs syndrome
 * Myomyectomy
 * Myometrial hypertrophy
 * Uterine diverticulum
 * Cervical diverticulum
 * Vulvar condyloma

Genetics

 * MyD88 deficiency
 * warfarin sensitivity
 * autosomal trisomy

Rare diseases

 * Acromesomelic dysplasia
 * Acute eosinophilic pneumonia
 * AIDS dysmorphic syndrome
 * Ameloblastic carcinoma
 * Infantile apnea
 * ATR-16 syndrome
 * Autosomal dominant porencephaly type I
 * Blepharophimosis, ptosis, epicanthus inversus syndrome
 * Chronic eosinophilic pneumonia (as a separate article)
 * Type 1 citrullinemia
 * Congenital bilateral perisylvian syndrome
 * Congenital lactic acidosis
 * Congenital pulmonary lymphangiectasia
 * Congenital varicella syndrome (as a separate article)
 * Craniometaphyseal dysplasia (covering both AD/AR inheritance)
 * Cytochrome C oxidase deficiency
 * De Santis Cacchione syndrome
 * Dentin dysplasia type I
 * Dentin dysplasia type II
 * Dentinogenesis imperfecta type III
 * Diffuse pulmonary lymphangiomatosis
 * Idiopathic dilatation of the pulmonary artery
 * Disaccharide intolerance I
 * Dyggve-Melchior-Clausen syndrome
 * Ear, Patella, Short Stature Syndrome
 * Factor VII deficiency (separate article)
 * Factor XII deficiency (separate article)
 * Familial eosinophilic cellulitis
 * Familial isolated hypoparathyroidism
 * Familial lipoprotein lipase deficiency
 * Femoral facial syndrome
 * Ferroportin disease
 * Fetal retinoid syndrome
 * Fetal valproate syndrome (separate article)
 * FG syndrome type 1
 * Filippi syndrome
 * Formaldehyde poisoning (separate)
 * Frontofacionasal dysplasia
 * Giant hypertrophic gastritis
 * General myoclonus
 * Goodman syndrome
 * Gorlin-Chaudhry-Moss Syndrome
 * Growth hormone insensitivity
 * Hereditary hyperphosphatasia
 * Hereditary multiple osteochondromas
 * Hereditary sensory and autonomic neuropathy type II
 * Human HOXA1 syndromes
 * Hyperferritinemia cataract syndrome
 * Hyperprolinemia type I
 * Hyperprolinemia type II
 * Idiopathic neonatal hepatitis
 * Idiopathic subglottic stenosis
 * IRF6-related disorders
 * KBG syndrome
 * Kenny-Caffey syndrome
 * LADD syndrome
 * Levy-Yeboa syndrome
 * Low gamma-GT familial intrahepatic cholestasis
 * Maxillofacial dysostosis
 * MDR3 deficiency
 * Neuhauser syndrome
 * Metatropic dysplasia I