Prepladder Notes 2026

*Prof sales from App/Website will end on 16th. Plan your sales accordingly* *Prof combo wil not be available after 16th* Also *Elite plan* prices will increase Thursday night *If anyone want to subscribe then do it ASAP*

Special Offer only for Prof Plan Use code "CKSNXQ9W" and get maximum cashback and discount CONT ME :- https://chat.whatsapp.com/Gt5jRWciSdkLANfTb3nAWh Starting Prof 1 + Prof 2 in just Rs 6,599 Rs for 12 Month Prof 1 + Prof 2 Plan 12 Month = 6,599 Rs 15 Month = 7,499 Rs 18 Month = 8,399 Rs

P R E P L🅰 D D ER HOLI buy 1 proff get 1 proff O F F E R We're happy to launch Prof-Wise subscription plans to fulfill your university exam requirements along with NEXT and INICET preparation. INCLUDES ✏️ ANATOMY ✏️ PHYSIOLOGY ✏️ BIOCHEMISTRY ✏️ PATHOLOGY ✏️PHARMACOLOGY ✏️MICROBIOLOGY 🥇 VIDEO LECTURES 🥈 QUESTION BANK 🏅 TEST SERIES 🥉 RAPID REVISION 🎖 CLINICAL CASE (1st+2nd)proff combo website price ₹10800 🎯 OFFER PRICE- ₹6999 To avail discount offer click on the link below and register now. (Limited code left) ☑️LINK- https://docs.google.com/forms/d/e/1FAIpQLSdCidkpFcYh-3ftu-lESv8vRAM3Vn79zLL9tKPN9smNjpDp-w/viewform?usp=pp_url Prepladder team Keyuer

*Prof is launched for few days only... It may be removed again... So those want to enroll, do it ASAP* Use code - MANA49D4

*Are you really risking it?* 😱 The chance to study from both the old and new Dream Team faculty members! Don’t let this happen. *Grab ELITE Plan Now* 👇🏻 prepladder.com/courses/medical-pg/plan *Use Code: PRANX23X* for additional benefits. *Because, the video lectures from the existing Dream Team won’t be available from March 6th, 2023 onwards.* ⏳ _PS: Old Dream Team video lectures will only be available for 13 subjects._ Team PrepLadder. Contact- 9532530063

✅HLA DR2 : SLE(Japanese) & Sjogren Syndrome ✅HLA DR3 : Type I diabetes mellitus,Dermatitis herpetiformis, Chronic active hepatitis, Sjogren's syndrome ,SLE (white) ✅HLA DR4 : Rhematiod Arthritis ✅HLA DR5 : Pernicious Anemia , Hasitimo's Thyroiditis ✅HLA DR8 ,DR5 : juvenile arthritis ( pauci articular) ✅Disorders related to chromosomes 🎯Chromosome 1: * Rh system  * Neuroblastoma 🎯Chromosome 2: *Cystinuria * Hypobetalipoproteinemi 🎯Chromosome 3: * RCC * ALKAPTONURIA 🎯Chromosome 4: * Huntingtons chorea * Achondroplasia * Parkinsons disease 🎯Chromosome 5: * FAP * Colorectal carcinoma * Cri-du-chat syndrome 🎯Chromosome 6: * HLA system(short arm) * MHA antigen * DM 🎯Chromosome 7: *Cystic fibrosis 🎯Chromosome 8: *Osteoporosis 🎯Chromosome 9: * ABO blood group * Friedreich’s ataxia 🎯Chromosome 10: * Apert syndrome * Charcot-Marie-Tooth disease * Cockayne syndrome * Congenital erythropoietic porphyria * Cowden syndrome    * Crouzon syndrome * Hirschprung disease * MEN-2 * Pfeiffer syndrome * porphyri Usher syndrome * Usher syndrome type I * Wolman syndrome 🎯Chromosome 11: * Sickle cell anaemia/ * Beta thallasemia * Wilms tumour/ * MEN -1 * Ataxia telengiectasia * Human insulin gene * PTH gene 🎯Chromosome 12: * PKU * vWF * CA testes 🎯Chromosome 13: * Retinoblastoma * Osteosarcoma * Wilsons ds * BRCA-2 🎯Chromosome 14: * Familial HOCM/ * alpha 1 antitripsin deficiency 🎯Chromosome 15: * Marfan’s syndrome * Albinism * Pradder willi syndrome * Angelman syndrome 🎯Chromosome 16: * Alpha thallasemia * Adult PKD 🎯chromosome 17: * Carninoma breast(BRCA1) * Medulloblastoma * Neurofibromatosis-1 * Ovarian tumour * p53 gene 🎯Chromosome 18: * Erythropoietic protoporphyria hereditary * Hemorrhagic telangiectasia * Niemann-Pick disease * Type C porphyria * Selective Mutism * Edwards syndrome (Trisomy 18) 🎯Chromosome 19: * Myotonia dystrophica * Gene for insulin receptor 🎯Chromosome 20: * MODY type 1 DM * Prions disease 🎯Chromosome 21: * Homocystinuria * Amyloidosis…folic acid transport.. 🎯Chromosome 22: * Meningioma * Acoustic neuroma * NF -2 * Di-George syndrome 🎯Chromosome Xq: * Gene for androgen insensitivity syndrome * Fragile X syndrome * Testicular feminisation * X-SCID * X linked agaamaglobulinemia * Fabry ds * Lesch- Nyhan * Hemophilia B * Hemophilia A * Hunter syndrome * G6PD deficiency 🎯Chromosome Xp – * Ocular albinism * Chr Granulomatous Ds * DMD * Menkes syndrome