The following pages link to Transient neonatal diabetes
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Complications of diabetes (links | edit)
- Type 3 diabetes (links | edit)
- List of people with type 1 diabetes (links | edit)
- Fluorescent glucose biosensor (links | edit)
- Prevention of type 2 diabetes (links | edit)
- Diabetic foot (links | edit)
- Genetic causes of type 2 diabetes (links | edit)
- Lifestyle causes of type 2 diabetes (links | edit)
- History of diabetes (links | edit)
- Epigenetics of diabetes type 2 (links | edit)
- First Nations and diabetes (links | edit)
- Ketosis-prone diabetes (links | edit)
- Epidemiology of diabetes (links | edit)
- Diabetes (links | edit)
- Diabetic foot ulcer (links | edit)
- Ambulatory glucose profile (links | edit)
- Type 3c diabetes (links | edit)
- Disposition index (links | edit)
- Diabetes and exercise (links | edit)
- Transient neonatal diabetes mellitus (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Genomic imprinting (links | edit)
- Neuromyotonia (links | edit)
- Cystic fibrosis (links | edit)
- Androgen insensitivity syndrome (links | edit)
- Adrenoleukodystrophy (links | edit)
- Prader–Willi syndrome (links | edit)
- List of diseases (N) (links | edit)
- Febrile seizure (links | edit)
- Brugada syndrome (links | edit)
- Langer–Giedion syndrome (links | edit)
- Lissencephaly (links | edit)
- Cleft lip and cleft palate (links | edit)
- Septo-optic dysplasia (links | edit)
- Tietz syndrome (links | edit)
- Congenital hypothyroidism (links | edit)
- Retinitis pigmentosa (links | edit)
- Long QT syndrome (links | edit)
- Harlequin-type ichthyosis (links | edit)
- Osteopetrosis (links | edit)
- XY gonadal dysgenesis (links | edit)
- Arrhythmogenic cardiomyopathy (links | edit)
- Dilated cardiomyopathy (links | edit)
- Congenital insensitivity to pain (links | edit)
- Waardenburg syndrome (links | edit)
- Lamellar ichthyosis (links | edit)
- Malignant hyperthermia (links | edit)
- Beckwith–Wiedemann syndrome (links | edit)
- Kabuki syndrome (links | edit)
- Erythromelalgia (links | edit)
- Maturity-onset diabetes of the young (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Hallermann–Streiff syndrome (links | edit)
- Li–Fraumeni syndrome (links | edit)
- Hyperkalemic periodic paralysis (links | edit)
- Thyroid hormone resistance (links | edit)
- Timothy syndrome (links | edit)
- Pickardt syndrome (links | edit)
- Non-Mendelian inheritance (links | edit)
- Rubinstein–Taybi syndrome (links | edit)
- Jervell and Lange-Nielsen syndrome (links | edit)
- Romano–Ward syndrome (links | edit)
- Andersen–Tawil syndrome (links | edit)
- Fuchs' dystrophy (links | edit)
- Hypoplastic left heart syndrome (links | edit)
- Saethre–Chotzen syndrome (links | edit)
- Spinal and bulbar muscular atrophy (links | edit)
- Channelopathy (links | edit)
- Sideroblastic anemia (links | edit)
- Myotonia congenita (links | edit)
- Dubin–Johnson syndrome (links | edit)
- Pseudoxanthoma elasticum (links | edit)
- Popliteal pterygium syndrome (links | edit)
- X-linked adrenal hypoplasia congenita (links | edit)
- Hypokalemic periodic paralysis (links | edit)
- Paramyotonia congenita (links | edit)
- Nonsyndromic deafness (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Pseudohypoparathyroidism (links | edit)
- Barakat syndrome (links | edit)
- Cleidocranial dysostosis (links | edit)
- Liddle's syndrome (links | edit)
- Bartter syndrome (links | edit)
- IPEX syndrome (links | edit)
- Progressive familial intrahepatic cholestasis (links | edit)
- Hyperimmunoglobulin E syndrome (links | edit)
- Ion transporter (links | edit)
- Primary ovarian insufficiency (links | edit)
- Greig cephalopolysyndactyly syndrome (links | edit)
- Vitelliform macular dystrophy (links | edit)
- Pallister–Hall syndrome (links | edit)
- Léri–Weill dyschondrosteosis (links | edit)
- Congenital absence of the vas deferens (links | edit)
- Holt–Oram syndrome (links | edit)
- Nail–patella syndrome (links | edit)
- Stargardt disease (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Tangier disease (links | edit)
- Duane-radial ray syndrome (links | edit)
- Mowat–Wilson syndrome (links | edit)
- Mucolipidosis type IV (links | edit)
- Pseudopseudohypoparathyroidism (links | edit)
- Denys–Drash syndrome (links | edit)
- Sitosterolemia (links | edit)
- Partial androgen insensitivity syndrome (links | edit)
- Ectrodactyly–ectodermal dysplasia–cleft syndrome (links | edit)
- Lymphedema–distichiasis syndrome (links | edit)
- Axenfeld–Rieger syndrome (links | edit)
- Generalized epilepsy with febrile seizures plus (links | edit)
- Benign familial neonatal seizures (links | edit)
- Catecholaminergic polymorphic ventricular tachycardia (links | edit)
- Papillorenal syndrome (links | edit)
- Spinocerebellar ataxia type 6 (links | edit)
- Campomelic dysplasia (links | edit)
- Episodic ataxia (links | edit)
- Spinocerebellar ataxia type-13 (links | edit)
- Estrogen insensitivity syndrome (links | edit)
- Congenital stationary night blindness (links | edit)
- Myotonic dystrophy (links | edit)
- Townes–Brocks syndrome (links | edit)
- Familial atrial fibrillation (links | edit)
- Hay–Wells syndrome (links | edit)
- Dent's disease (links | edit)
- Currarino syndrome (links | edit)
- Potassium-aggravated myotonia (links | edit)
- Feingold syndrome (links | edit)
- Paroxysmal extreme pain disorder (links | edit)
- Ohtahara syndrome (links | edit)
- Oculodentodigital dysplasia (links | edit)
- Central core disease (links | edit)
- Acrocallosal syndrome (links | edit)
- Ocular albinism (links | edit)
- Angelman syndrome (links | edit)
- Iridogoniodysgenesis, dominant type (links | edit)
- X-linked intellectual disability (links | edit)
- Ichthyosis hystrix (links | edit)
- Erythrokeratodermia variabilis (links | edit)
- Keratitis–ichthyosis–deafness syndrome (links | edit)
- Atrichia with papular lesions (links | edit)
- Clouston's hidrotic ectodermal dysplasia (links | edit)
- Rapp–Hodgkin syndrome (links | edit)
- Tooth and nail syndrome (links | edit)
- Synpolydactyly (links | edit)
- Progressive symmetric erythrokeratodermia (links | edit)
- Familial partial lipodystrophy (links | edit)
- Autoimmune polyendocrine syndrome type 1 (links | edit)
- Gillespie syndrome (links | edit)
- MODY 1 (links | edit)
- MODY 3 (links | edit)
- MODY 4 (links | edit)
- Renal cysts and diabetes syndrome (links | edit)
- Permanent neonatal diabetes (links | edit)
- Transient neonatal diabetes (links | edit)
- EAST syndrome (links | edit)
- Enlarged vestibular aqueduct (links | edit)
- Neonatal diabetes (links | edit)
- MODY 6 (links | edit)
- Yemenite deaf-blind hypopigmentation syndrome (links | edit)
- Ulnar–mammary syndrome (links | edit)
- Anterior segment mesenchymal dysgenesis (links | edit)
- Complete androgen insensitivity syndrome (links | edit)
- Alveolar capillary dysplasia (links | edit)
- Pitt–Hopkins syndrome (links | edit)
- Bart–Pumphrey syndrome (links | edit)
- Silver–Russell syndrome (links | edit)
- Bamforth–Lazarus syndrome (links | edit)
- Limb–mammary syndrome (links | edit)
- Mild androgen insensitivity syndrome (links | edit)
- Thyrotoxic periodic paralysis (links | edit)
- ZFP57 (links | edit)
- Surfactant metabolism dysfunction (links | edit)
- Hypotrichosis–lymphedema–telangiectasia syndrome (links | edit)
- HYMAI (links | edit)
- Aromatase excess syndrome (links | edit)
- Leydig cell hypoplasia (links | edit)
- Follicle-stimulating hormone insensitivity (links | edit)
- Emily's Entourage (links | edit)
- Temple–Baraitser syndrome (links | edit)
- Generalized glucocorticoid resistance (links | edit)
- Talk:Transient neonatal diabetes mellitus (transclusion) (links | edit)
- User:AlexNewArtBot/GeneticsSearchResult/archive1 (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive20 (links | edit)
- User:Katiekillick/sandbox (links | edit)
- User:ChristianLugar/sandbox (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages (links | edit)
- User:Drsalmanshah165/Books/Anaphylaxis (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-N (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-O (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-pha (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia0-pln (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-P (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-Q (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-R (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-S (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-T (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-U (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-V (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-W (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-X (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-Y (links | edit)
- User:Drsalmanshah165/Books/Medical Misplaced Pages 0-z (links | edit)
- User:Drsalmanshah165/Books/Medical wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Misplaced Pages (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Misplaced Pages 0-Z (links | edit)
- User:Chris3922/sandbox (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:TGriggs2/sandbox (links | edit)
- User:Jcrank07/sandbox (links | edit)
- User:Pdesai93/sandbox (links | edit)
- User:Nihlus/sandbox 3 (links | edit)
- User:Yaqi Zhao/sandbox/Channelopathy/skeleton muscle (links | edit)
- User talk:Daniel Mietchen/SuggestBot/Archive 1 (links | edit)
- User talk:Daniel Mietchen/SuggestBot/Total (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Template:Genomic imprinting (links | edit)
- Template:Transcription factor and coregulator deficiencies (links | edit)
- Template:Channelopathy (links | edit)
- Template:ABC transporter disorders (links | edit)
- ZNF337 (links | edit)
- Diabetic embryopathy (links | edit)
- Dasiglucagon (links | edit)
- Insulin icodec (links | edit)
- SPINA-GR (links | edit)
- SPINA-GBeta (links | edit)
- Pancreatic beta cell function (links | edit)
- Diabetes mellitus, transient neonatal (redirect page) (links | edit)
- Talk:Transient neonatal diabetes (transclusion) (links | edit)
- User:TGriggs2/sandbox (links | edit)
- User:Ggrear/sandbox (links | edit)
- User:MimiGregg/sandbox (links | edit)
- User:Y-S.Ko/Wikipedia course/Medical/Endocrinology (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Short descriptions/wd/diseases (links | edit)
- Misplaced Pages:WikiProject Medicine/The ICD-11 coding challenge/5300–5399 (links | edit)
- Template:Diabetes (links | edit)
- Category:Diabetes (links | edit)