| Disease Name |
Symbol |
Acronym |
| L-2-Hydroxyglutaric Aciduria |
L2H001 |
L2HGA |
| La Crosse Encephalitis |
LCR004 |
|
| Labia Minora Cancer |
LBM005 |
|
| Labia Minora, Incomplete Adhesion of |
LBM006 |
|
| Labium Majus Cancer |
LBM004 |
|
| Labrador Lung |
LBR003 |
|
| Labyrinthine Bilateral Reactive Loss |
LBY002 |
|
| Labyrinthine Unilateral Reactive Loss |
LBY001 |
|
| Labyrinthitis |
LBY004 |
|
| Lachiewicz Sibley Syndrome |
LCH006 |
|
| Lacrimal Apparatus Disease |
LCR008 |
|
| Lacrimal Drainage System Anomaly |
LCR016 |
|
| Lacrimal Drainage System Anomaly of Genetic Origin |
LCR015 |
|
| Lacrimal Duct Cancer |
LCR005 |
|
| Lacrimal Duct Defect |
LCR013 |
LCDD |
| Lacrimal Duct Obstruction |
LCR001 |
|
| Lacrimal Gland Adenocarcinoma |
LCR009 |
|
| Lacrimal Gland Adenoid Cystic Carcinoma |
LCR006 |
|
| Lacrimal Gland Carcinoma |
LCR011 |
|
| Lacrimal Gland Mucoepidermoid Carcinoma |
LCR002 |
|
| Lacrimal Gland Squamous Cell Carcinoma |
LCR007 |
|
| Lacrimal Passage Granuloma |
LCR003 |
|
| Lacrimal System Cancer |
LCR012 |
|
| Lacrimoauriculodentodigital Syndrome |
LCR014 |
LADD |
| Lactase Deficiency, Congenital |
LCT013 |
COLACD |
| Lactate Dehydrogenase B Deficiency |
LCT017 |
LDHBD |
| Lactate Dehydrogenase Deficiency |
LCT008 |
|
| Lactic Acidosis |
LCT001 |
|
| Lactic Acidosis Congenital Infantile |
LCT010 |
|
| Lactic Acidosis, Chronic Adult Form |
LCT020 |
|
| Lactobezoar |
LCT018 |
|
| Lactocele |
LCT003 |
|
| Lactose Intolerance |
LCT002 |
|
| Lactose Intolerance, Adult Type |
LCT011 |
|
| Lagophthalmos |
LGP001 |
|
| Lama2-Related Muscular Dystrophy |
LM2001 |
|
| Lama5-Related Multisystemic Syndrome |
LM5001 |
|
| Lambda 5 Deficiency |
LMB004 |
|
| Lambdoid Synostosis |
LMB009 |
|
| Lambert Syndrome |
LMB010 |
|
| Lambert-Eaton Myasthenic Syndrome |
LMB002 |
LEMS |
| Lambotte Syndrome |
LMB071 |
|
| Lamb-Shaffer Syndrome |
LMB069 |
LAMSHF |
| Laminin Subunit Alpha 2-Related Congenital Muscular Dystrophy |
LMN012 |
|
| Laminin Subunit Alpha 2-Related Limb-Girdle Muscular Dystrophy R23 |
LMN014 |
|
| Laminin Subunit Alpha 2-Related Muscular Dystrophy |
LMN013 |
|
| Laminopathy |
LMN011 |
|
| Laminopathy with Lipodystrophy |
LMN008 |
|
| Laminopathy with Peripheral Neuropathy |
LMN009 |
|
| Laminopathy with Premature Aging |
LMN010 |
|
| Laminopathy with Striated Muscle Involvement |
LMN007 |
|
| Landau-Kleffner Syndrome |
LND001 |
LKS |
| Landy-Donnai Syndrome |
LND002 |
|
| Langer Mesomelic Dysplasia |
LNG040 |
LMD |
| Langerhans Cell Histiocytosis |
LNG108 |
LCH |
| Langerhans Cell Sarcoma |
LNG004 |
|
| Language Delay and Attention Deficit-Hyperactivity Disorder/cognitive Impairment with or Without Cardiac Arrhythmia |
LNG104 |
LADCI |
| Large Bowel Leiomyoma |
LRG006 |
|
| Large Cell Acanthoma |
LRG002 |
|
| Large Cell Carcinoma |
LRG001 |
|
| Large Cell Carcinoma with Rhabdoid Phenotype |
LRG005 |
|
| Large Cell Keratinizing Variant Squamous Cell Breast Carcinoma |
LRG004 |
|
| Large Cell Medulloblastoma |
LRG003 |
|
| Large Cell Neuroendocrine Carcinoma |
LRG014 |
|
| Large Congenital Melanocytic Nevus |
LRG012 |
GMN |
| Large Granular Lymphocyte Leukemia |
LRG008 |
|
| Large Intestine Adenocarcinoma |
LRG016 |
|
| Large Intestine Adenoma |
LRG015 |
|
| Large Intestine Cancer |
LRG017 |
|
| Large Intestine Lipoma |
LRG007 |
|
| L-Arginine:glycine Amidinotransferase Deficiency |
LRG010 |
|
| Laron Syndrome |
LRN002 |
LARS |
| Larsen Syndrome |
LRS001 |
LRS |
| Larsen-Like Syndrome |
LRS002 |
LRSL |
| Larsen-Like Syndrome B3gat3 Type |
LRS010 |
|
| Larsen-Like Syndrome, Lethal Type |
LRS009 |
|
| Laryngeal Abductor Paralysis |
LRY047 |
LABD |
| Laryngeal Abductor Paralysis with Cerebellar Ataxia and Motor Neuropathy |
LRY052 |
|
| Laryngeal Abductor Paralysis-Intellectual Disability Syndrome |
LRY045 |
|
| Laryngeal Adductor Paralysis |
LRY021 |
LAP |
| Laryngeal Adenoid Cystic Carcinoma |
LRY010 |
|
| Laryngeal Atresia, Encephalocele, and Limb Deformities |
LRY053 |
LEL |
| Laryngeal Benign Neoplasm |
LRY015 |
|
| Laryngeal Cartilage Cancer |
LRY012 |
|
| Laryngeal Cleft |
LRY026 |
LC |
| Laryngeal Disease |
LRY017 |
|
| Laryngeal Mucoepidermoid Carcinoma |
LRY003 |
|
| Laryngeal Neuroendocrine Tumor |
LRY013 |
|
| Laryngeal Papillomatosis |
LRY027 |
|
| Laryngeal Small Cell Carcinoma |
LRY005 |
|
| Laryngeal Squamous Cell Carcinoma |
LRY018 |
|
| Laryngeal Tuberculosis |
LRY007 |
|
| Laryngeal Web, Familial |
LRY046 |
|
| Laryngitis |
LRY019 |
|
| Laryngocele |
LRY028 |
|
| Laryngomalacia |
LRY029 |
|
| Laryngoonychocutaneous Syndrome |
LRY022 |
LOCS |
| Laryngostenosis |
LRY002 |
|
| Laryngotracheal Angioma |
LRY034 |
|
| Laryngotracheitis |
LRY004 |
|
| Laryngotracheoesophageal Cleft Type 0 |
LRY048 |
LTEC0 |
| Laryngotracheoesophageal Cleft Type 1 |
LRY051 |
LTEC1 |
| Laryngotracheoesophageal Cleft Type 2 |
LRY050 |
LTEC2 |
| Laryngotracheoesophageal Cleft Type 4 |
LRY049 |
LTEC4 |
| Larynx Anomaly |
LRY054 |
|
| Larynx Atresia |
LRY030 |
|
| Larynx Cancer |
LRY044 |
|
| Larynx Carcinoma in Situ |
LRY009 |
|
| Larynx Leiomyoma |
LRY001 |
|
| Larynx Leiomyosarcoma |
LRY014 |
|
| Larynx Liposarcoma |
LRY008 |
|
| Larynx Sarcoma |
LRY020 |
|
| Larynx Squamous Papilloma |
LRY006 |
|
| Larynx Verrucous Carcinoma |
LRY011 |
|
| Larynx, Congenital Partial Atresia of |
LRY031 |
|
| Lassa Fever |
LSS003 |
LF |
| Late Congenital Syphilis |
LTC001 |
|
| Late Yaws |
LTY001 |
|
| Late-Infantile/juvenile Krabbe Disease |
LTN017 |
|
| Latent Syphilis |
LTN001 |
|
| Late-Onset Ataxia with Dementia |
LTN027 |
|
| Late-Onset Distal Myopathy, Markesbery-Griggs Type |
LTN022 |
|
| Late-Onset Familial Hypoaldosteronism |
LTN026 |
|
| Late-Onset Focal Dermal Elastosis |
LTN013 |
|
| Late-Onset Isolated Acth Deficiency |
LTN011 |
|
| Late-Onset Junctional Epidermolysis Bullosa |
LTN015 |
|
| Late-Onset Localized Junctional Epidermolysis Bullosa-Intellectual Disability Syndrome |
LTN023 |
|
| Late-Onset Nephronophthisis |
LTN020 |
|
| Late-Onset Primary Lymphedema Without Systemic or Visceral Involvement |
LTN028 |
|
| Late-Onset Retinal Degeneration |
LTN004 |
LORD |
| Late-Onset Scapuloperoneal Muscular Dystrophy with Hyaline Bodies |
LTN025 |
|
| Lateral Cystocele |
LTR006 |
|
| Lateral Displacement of Eye |
LTR005 |
|
| Lateral Facial Cleft |
LTR017 |
|
| Lateral Medullary Syndrome |
LTR003 |
|
| Lateral Meningocele Syndrome |
LTR009 |
LMNS |
| Lateral Myocardial Infarction |
LTR004 |
|
| Lateral Sclerosis |
LTR001 |
|
| Lateral Semicircular Canal Malformation, Familial, with External and Middle Ear Abnormalities |
LTR010 |
|
| Lateral Sinus Thrombosis |
LTR002 |
|
| Lateral Ventricle Meningioma |
LTR007 |
|
| Laterality Defects Dominant |
LTR011 |
|
| Latex Allergy |
LTX001 |
|
| Lathosterolosis |
LTH002 |
LATHST |
| Lathyrism |
LTH004 |
|
| Lattice Corneal Dystrophy |
LTT001 |
|
| Lattice Corneal Dystrophy Type Ii |
LTT008 |
|
| Lattice Degeneration of Retina Leading to Retinal Detachment |
LTT009 |
|
| Laubry-Pezzi Syndrome |
LBR027 |
|
| Laugier-Hunziker Syndrome |
LGR001 |
LHS |
| Laurence-Moon Syndrome |
LRN001 |
LNMS |
| Laurin-Sandrow Syndrome |
LRN006 |
LSS |
| Lazy Leukocyte Syndrome |
LZY001 |
|
| L-Cell Glucagon-Like Peptide Producing Tumor |
LCL008 |
|
| Le Marec Bracq Picaud Syndrome |
LMR002 |
|
| Lean Body Mass Quantitative Trait Locus 1 |
LNB002 |
LBMQTL1 |
| Learning Disability |
LRN003 |
|
| Leber Congenital Amaurosis |
LBR001 |
CRB |
| Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy |
LBR033 |
LCA |
| Leber Congenital Amaurosis 1 |
LBR004 |
LCA1 |
| Leber Congenital Amaurosis 10 |
LBR005 |
LCA10 |
| Leber Congenital Amaurosis 11 |
LBR006 |
LCA11 |
| Leber Congenital Amaurosis 12 |
LBR007 |
LCA12 |
| Leber Congenital Amaurosis 13 |
LBR008 |
LCA13 |
| Leber Congenital Amaurosis 14 |
LBR009 |
LCA14 |
| Leber Congenital Amaurosis 15 |
LBR010 |
LCA15 |
| Leber Congenital Amaurosis 16 |
LBR011 |
LCA16 |
| Leber Congenital Amaurosis 17 |
LBR029 |
LCA17 |
| Leber Congenital Amaurosis 19 |
LBR034 |
LCA19 |
| Leber Congenital Amaurosis 2 |
LBR012 |
LCA2 |
| Leber Congenital Amaurosis 3 |
LBR013 |
LCA3 |
| Leber Congenital Amaurosis 4 |
LBR014 |
LCA4 |
| Leber Congenital Amaurosis 5 |
LBR015 |
LCA5 |
| Leber Congenital Amaurosis 6 |
LBR016 |
LCA6 |
| Leber Congenital Amaurosis 7 |
LBR017 |
LCA7 |
| Leber Congenital Amaurosis 8 |
LBR018 |
LCA8 |
| Leber Congenital Amaurosis 9 |
LBR019 |
LCA9 |
| Leber Congenital Amaurosis with Early-Onset Deafness |
LBR032 |
LCAEOD |
| Leber Optic Atrophy |
LBR030 |
LHON |
| Leber Optic Atrophy and Dystonia |
LBR031 |
LDYT |
| Lecithin:cholesterol Acyltransferase Deficiency |
LCT022 |
LCATD |
| Ledderhose Disease |
LDD006 |
|
| Leech Infestation |
LCH001 |
|
| Left Bundle Branch Hemiblock |
LFT001 |
|
| Left Sided Atrial Isomerism |
LFT022 |
LAI |
| Left Ventricular Noncompaction |
LFT003 |
LVHT |
| Left Ventricular Noncompaction 1 |
LFT021 |
LVNC1 |
| Left Ventricular Noncompaction 10 |
LFT018 |
LVNC10 |
| Left Ventricular Noncompaction 2 |
LFT011 |
LVNC2 |
| Left Ventricular Noncompaction 7 |
LFT020 |
LVNC7 |
| Left Ventricular Noncompaction 8 |
LFT017 |
LVNC8 |
| Left-Sided Gallbladder |
LFT005 |
|
| Leg Absence Deformity Cataract |
LGB001 |
|
| Leg Dermatosis |
LGD001 |
|
| Leg Ulcers, Familial, of Juvenile Onset |
LGL002 |
|
| Leg, Absence Deformity of, with Congenital Cataract |
LGB002 |
|
| Legg-Calve-Perthes Disease |
LGG001 |
LCPD |
| Legionellosis |
LGN002 |
|
| Legionnaire Disease |
LGN006 |
|
| Legius Syndrome |
LGS001 |
LGSS |
| Legume Allergy |
LGM010 |
|
| Leigh Syndrome |
LGH007 |
LS |
| Leigh Syndrome with Cardiomyopathy |
LGH013 |
|
| Leigh Syndrome with Leukodystrophy |
LGH012 |
|
| Leigh Syndrome with Nephrotic Syndrome |
LGH017 |
|
| Leigh Syndrome, French Canadian Type |
LGH003 |
LSFC |
| Leiner Disease |
LNR001 |
|
| Leiomyoma |
LMY002 |
|
| Leiomyoma Cutis |
LMY001 |
|
| Leiomyoma of Vulva and Esophagus |
LMY006 |
|
| Leiomyoma, Uterine |
LMY014 |
UL |
| Leiomyomatosis |
LMY003 |
|
| Leiomyomatosis of Esophagus, Cataract and Hematuria |
LMY008 |
|
| Leiomyomatosis, Diffuse, with Alport Syndrome |
LMY010 |
DL-ATS |
| Leiomyosarcoma |
LMY004 |
|
| Leiomyosarcoma of the Cervix Uteri |
LMY012 |
|
| Leishmaniasis |
LSH001 |
|
| Leishmaniasis, Tegumentary |
LSH003 |
|
| Lelis Syndrome |
LLS001 |
|
| Lemierre's Syndrome |
LMR001 |
|
| Lennox-Gastaut Syndrome |
LNN001 |
LGS |
| Lens Disease |
LNS003 |
|
| Lens Position Anomaly |
LNS008 |
|
| Lens Position Anomaly of Genetic Origin |
LNS005 |
|
| Lens Shape Anomaly |
LNS007 |
|
| Lens Size Anomaly |
LNS009 |
|
| Lens Size Anomaly of Genetic Origin |
LNS006 |
|
| Lens Subluxation |
LNS001 |
|
| Lens-Induced Iridocyclitis |
LNS002 |
|
| Lentigines |
LNT004 |
|
| Lentiginosis, Centrofacial Neurodysraphic |
LNT009 |
|
| Lentiginosis, Inherited Patterned |
LNT008 |
|
| Lentigo Maligna Melanoma |
LNT002 |
LMM |
| Lenz-Majewski Hyperostotic Dwarfism |
LNZ003 |
LMHD |
| Leopard Syndrome |
LPR002 |
NSML |
| Leopard Syndrome 1 |
LPR012 |
LPRD1 |
| Leopard Syndrome 2 |
LPR011 |
LPRD2 |
| Leopard Syndrome 3 |
LPR007 |
LPRD3 |
| Lepromatous Leprosy |
LPR001 |
|
| Leprosy 1 |
LPR023 |
LPRS1 |
| Leprosy 2 |
LPR022 |
LPRS2 |
| Leprosy 3 |
LPR021 |
LPRS3 |
| Leprosy 4 |
LPR016 |
LPRS4 |
| Leprosy 5 |
LPR017 |
LPRS5 |
| Leprosy 6 |
LPR020 |
LPRS6 |
| Leptin Deficiency or Dysfunction |
LPT014 |
LEPD |
| Leptin Receptor Deficiency |
LPT006 |
LEPRD |
| Leptin, Serum Level of, Quantitative Trait Locus 1 |
LPT013 |
LEPQTL1 |
| Leptomeninges Sarcoma |
LPT003 |
|
| Leptomyelolipoma |
LPT012 |
|
| Leptospirosis |
LPT001 |
|
| Leri-Weill Dyschondrosteosis |
LRW001 |
LWD |
| Lesch-Nyhan Phenotype with Normal Hgprt |
LSC004 |
|
| Lesch-Nyhan Syndrome |
LSC001 |
LNS |
| Lesion of Sciatic Nerve |
LSN001 |
|
| Lessel-Kubisch Syndrome |
LSS041 |
LSKB |
| Lethal Chondrodysplasia |
LTH050 |
|
| Lethal Chondrodysplasia Moerman Type |
LTH005 |
|
| Lethal Chondrodysplasia Seller Type |
LTH006 |
|
| Lethal Congenital Contracture Syndrome |
LTH003 |
LCCS |
| Lethal Congenital Contracture Syndrome 1 |
LTH007 |
LCCS1 |
| Lethal Congenital Contracture Syndrome 10 |
LTH042 |
LCCS10 |
| Lethal Congenital Contracture Syndrome 11 |
LTH039 |
LCCS11 |
| Lethal Congenital Contracture Syndrome 2 |
LTH008 |
LCCS2 |
| Lethal Congenital Contracture Syndrome 3 |
LTH047 |
LCCS3 |
| Lethal Congenital Contracture Syndrome 4 |
LTH026 |
LCCS4 |
| Lethal Congenital Contracture Syndrome 5 |
LTH027 |
LCCS5 |
| Lethal Congenital Contracture Syndrome 6 |
LTH031 |
LCCS6 |
| Lethal Congenital Contracture Syndrome 7 |
LTH032 |
LCCS7 |
| Lethal Congenital Contracture Syndrome 8 |
LTH030 |
LCCS8 |
| Lethal Congenital Contracture Syndrome 9 |
LTH029 |
LCCS9 |
| Lethal Hydranencephaly-Diaphragmatic Hernia Syndrome |
LTH040 |
|
| Lethal Midline Granuloma |
LTH001 |
NKTCL |
| Lethal Multiple Congenital Anomalies/dysmorphic Syndrome |
LTH049 |
|
| Lethal Neonatal Spasticity-Epileptic Encephalopathy Syndrome |
LTH036 |
|
| Lethal Short-Limb Skeletal Dysplasia, Al Gazali Type |
LTH046 |
|
| Letrozole Toxicity |
LTR016 |
|
| Letterer-Siwe Disease |
LTT002 |
LESD |
| Leukemia |
LKM002 |
|
| Leukemia, Acute Lymphoblastic |
LKM062 |
ALL |
| Leukemia, Acute Lymphoblastic 2 |
LKM055 |
ALL2 |
| Leukemia, Acute Lymphoblastic 3 |
LKM060 |
ALL3 |
| Leukemia, Acute Monocytic |
LKM070 |
|
| Leukemia, Acute Myelocytic, with Polyposis Coli and Colon Cancer |
LKM072 |
|
| Leukemia, Acute Myeloid |
LKM061 |
AML |
| Leukemia, Acute, X-Linked |
LKM073 |
|
| Leukemia, Chronic Lymphocytic |
LKM071 |
CLL |
| Leukemia, Chronic Lymphocytic 1 |
LKM050 |
CLLS1 |
| Leukemia, Chronic Lymphocytic 2 |
LKM056 |
DBM |
| Leukemia, Chronic Lymphocytic 3 |
LKM051 |
CLLS3 |
| Leukemia, Chronic Lymphocytic 4 |
LKM053 |
CLLS4 |
| Leukemia, Chronic Lymphocytic 5 |
LKM052 |
CLLS5 |
| Leukemia, Chronic Myeloid |
LKM063 |
CML |
| Leukocoria |
LKC002 |
|
| Leukocyte Adhesion Deficiency, Type I |
LKC009 |
LAD |
| Leukocyte Adhesion Deficiency, Type Iii |
LKC005 |
LAD3 |
| Leukocyte Antigen Group Five |
LKC011 |
LAG5 |
| Leukocyte Disease |
LKC003 |
|
| Leukocyte Nuclear Appendages, Hereditary Prevalence of |
LKC010 |
|
| Leukodystrophy |
LKD001 |
|
| Leukodystrophy and Acquired Microcephaly with or Without Dystonia |
LKD024 |
LDAMD |
| Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant |
LKD025 |
ADLD |
| Leukodystrophy, Hypomyelinating, 10 |
LKD020 |
HLD10 |
| Leukodystrophy, Hypomyelinating, 11 |
LKD021 |
HLD11 |
| Leukodystrophy, Hypomyelinating, 12 |
LKD023 |
HLD12 |
| Leukodystrophy, Hypomyelinating, 13 |
LKD022 |
HLD13 |
| Leukodystrophy, Hypomyelinating, 14 |
LKD027 |
HLD14 |
| Leukodystrophy, Hypomyelinating, 15 |
LKD028 |
HLD15 |
| Leukodystrophy, Hypomyelinating, 16 |
LKD029 |
HLD16 |
| Leukodystrophy, Hypomyelinating, 17 |
LKD030 |
HLD17 |
| Leukodystrophy, Hypomyelinating, 18 |
LKD031 |
HLD18 |
| Leukodystrophy, Hypomyelinating, 19, Transient Infantile |
LKD032 |
HLD19 |
| Leukodystrophy, Hypomyelinating, 2 |
LKD010 |
HLD2 |
| Leukodystrophy, Hypomyelinating, 3 |
LKD015 |
HLD3 |
| Leukodystrophy, Hypomyelinating, 4 |
LKD008 |
HLD4 |
| Leukodystrophy, Hypomyelinating, 5 |
LKD009 |
HLD5 |
| Leukodystrophy, Hypomyelinating, 6 |
LKD019 |
HLD6 |
| Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism |
LKD017 |
HLD7 |
| Leukodystrophy, Hypomyelinating, 8, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism |
LKD018 |
HLD8 |
| Leukodystrophy, Hypomyelinating, 9 |
LKD016 |
HLD9 |
| Leukodystrophy, Progressive, Early Childhood-Onset |
LKD026 |
PLDECO |
| Leukoencephalopathy Palmoplantar Keratoderma |
LKN004 |
|
| Leukoencephalopathy with Ataxia |
LKN017 |
LKPAT |
| Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation |
LKN026 |
LBSL |
| Leukoencephalopathy with Dystonia and Motor Neuropathy |
LKN010 |
LKDMN |
| Leukoencephalopathy with Vanishing White Matter |
LKN001 |
VWM |
| Leukoencephalopathy, Acute Reversible, with Increased Urinary Alpha-Ketoglutarate |
LKN027 |
ARLIAK |
| Leukoencephalopathy, Arthritis, Colitis, and Hypogammaglobulinema |
LKN005 |
LACH |
| Leukoencephalopathy, Brain Calcifications, and Cysts |
LKN024 |
LCC |
| Leukoencephalopathy, Cerebral Calcifications, and Cysts |
LKN006 |
LCC |
| Leukoencephalopathy, Cystic, Without Megalencephaly |
LKN008 |
LCWM |
| Leukoencephalopathy, Hereditary Diffuse, with Spheroids |
LKN025 |
HDLS |
| Leukoencephalopathy, Progressive, with Ovarian Failure |
LKN018 |
LKENP |
| Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis |
LKM069 |
|
| Leukonychia Totalis-Acanthosis-Nigricans-Like Lesions-Abnormal Hair Syndrome |
LKN022 |
|
| Leukoplakia |
LKP003 |
|
| Leukoplakia of Penis |
LKP001 |
|
| Leukoplakia of Vagina |
LKP002 |
|
| Leukoregulin |
LKR002 |
|
| Leukorrhea |
LKR001 |
|
| Leukostasis |
LKS001 |
|
| Leukotriene C4 Synthase Deficiency |
LKT001 |
|
| Levator Syndrome |
LVT001 |
|
| Levator-Medial Rectus Synkinesis |
LVT003 |
|
| Levic Stefanovic Nikolic Syndrome |
LVC001 |
|
| Levocardia |
LVC002 |
|
| Levotransposition of the Great Arteries |
LVT002 |
|
| Lewis-Sumner Syndrome |
LWS001 |
|
| Leydig Cell Hypoplasia |
LYD011 |
LCH |
| Leydig Cell Hypoplasia, Type I |
LYD012 |
LHR |
| Leydig Cell Tumor |
LYD001 |
|
| L-Ferritin Deficiency |
LFR008 |
LFTD |
| Liang-Wang Syndrome |
LNG113 |
LIWAS |
| Lice Infestation |
LCN001 |
|
| Lichen Amyloidosis |
LCH014 |
|
| Lichen Disease |
LCH004 |
|
| Lichen Nitidus |
LCH003 |
|
| Lichen Planus |
LCH002 |
|
| Lichen Planus Pemphigoides |
LCH013 |
|
| Lichen Planus Pigmentosus |
LCH008 |
|
| Lichen Planus, Familial |
LCH017 |
|
| Lichen Sclerosus Et Atrophicus |
LCH016 |
LSA |
| Lichtenstein Syndrome |
LCH010 |
|
| Lichtenstein-Knorr Syndrome |
LCH015 |
LIKNS |
| Liddle Syndrome 1 |
LDD007 |
LIDLS1 |
| Liddle Syndrome 2 |
LDD008 |
LIDLS2 |
| Liddle Syndrome 3 |
LDD009 |
LIDLS3 |
| Lidocaine Allergy |
LDC001 |
|
| Liebenberg Syndrome |
LBN004 |
LBNBG |
| Li-Fraumeni Syndrome |
LFR001 |
LFS |
| Li-Fraumeni Syndrome 1 |
LFR009 |
LFS1 |
| Li-Fraumeni Syndrome 2 |
LFR007 |
LFS2 |
| Lig4 Syndrome |
LG4001 |
LIG4S |
| Light and Heavy Chain Deposition Disease |
LGH014 |
LHCDD |
| Light Chain Deposition Disease |
LGH004 |
LCDD |
| Light Fixation Seizure Syndrome |
LGH019 |
LFSS |
| Ligneous Conjunctivitis |
LGN005 |
|
| Limb Defects, Distal Transverse, with Mental Retardation and Spasticity |
LMB066 |
|
| Limb Ischemia |
LMB062 |
|
| Limbal Stem Cell Deficiency |
LMB050 |
|
| Limb-Body Wall Complex |
LMB014 |
|
| Limb-Girdle Muscular Dystrophy |
LMB006 |
LGMD |
| Limb-Girdle Muscular Dystrophy Type 1a |
LMB073 |
LGMD1 |
| Limb-Girdle Muscular Dystrophy Type 1b |
LMB074 |
|
| Limb-Girdle Muscular Dystrophy Type 1c |
LMB030 |
|
| Limbic Encephalitis |
LMB024 |
|
| Limbic Encephalitis Associated with Antibodies to Cell Membrane Antigens |
LMB075 |
|
| Limbic Encephalitis with Caspr2 Antibodies |
LMB058 |
|
| Limbic Encephalitis with Dpp6 Antibodies |
LMB060 |
|
| Limbic Encephalitis with Lgi1 Antibodies |
LMB053 |
|
| Limbic Encephalitis with Neurexin-3 Antibodies |
LMB072 |
|
| Limbic Encephalitis with Nmda Receptor Antibodies |
LMB059 |
|
| Limb-Mammary Syndrome |
LMB008 |
LMS |
| Limited Scleroderma |
LMT001 |
|
| Linear Atrophoderma of Moulin |
LNR009 |
|
| Linear Focal Elastosis |
LNR017 |
|
| Linear Hamartoma Syndrome |
LNR002 |
|
| Linear Iga Disease |
LNR006 |
LAD |
| Linear Lichen Planus |
LNR010 |
LLP |
| Linear Porokeratosis |
LNR004 |
|
| Linear Scleroderma |
LNR005 |
|
| Linear Skin Defects with Multiple Congenital Anomalies 1 |
LNR013 |
LSDMCA1 |
| Linear Skin Defects with Multiple Congenital Anomalies 2 |
LNR016 |
LSDMCA2 |
| Linear Skin Defects with Multiple Congenital Anomalies 3 |
LNR014 |
LSDMCA3 |
| Linear Verrucous Nevus Syndrome |
LNR012 |
|
| Lin-Gettig Syndrome |
LNG103 |
|
| Lingual Goiter |
LNG018 |
|
| Lingual-Facial-Buccal Dyskinesia |
LNG015 |
|
| Linitis Plastica |
LNT001 |
|
| Lip and Oral Cavity Cancer |
LPN002 |
|
| Lip Cancer |
LPC002 |
|
| Lip Carcinoma in Situ |
LPC001 |
|
| Lip Prints |
LPP007 |
|
| Lip, Hamartomatous |
LPH001 |
|
| Lip, Median Nodule of Upper |
LPM011 |
|
| Lipase Deficiency, Combined |
LPS020 |
CLD |
| Lipedema |
LPD026 |
|
| Lipedematous Scalp |
LPD038 |
|
| Lipid Metabolism Disorder |
LPD008 |
|
| Lipid Pneumonia |
LPD001 |
|
| Lipid Storage Disease |
LPD009 |
|
| Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency |
LPD042 |
LSMFLAD |
| Lipid-Cell Variant Infiltrating Bladder Urothelial Carcinoma |
LPD005 |
|
| Lipidosis with Triglycerid Storage Disease |
LPD013 |
|
| Lipid-Rich Breast Carcinoma |
LPD002 |
|
| Lipid-Rich Carcinoma |
LPD003 |
|
| Lipoadenoma |
LPD007 |
|
| Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules |
LPT004 |
LDHCP |
| Lipoblastoma |
LPB001 |
|
| Lipodermatosclerosis |
LPD014 |
|
| Lipodystrophy, Congenital Generalized, Type 1 |
LPD032 |
CGL1 |
| Lipodystrophy, Congenital Generalized, Type 2 |
LPD033 |
CGL2 |
| Lipodystrophy, Congenital Generalized, Type 3 |
LPD020 |
CGL3 |
| Lipodystrophy, Congenital Generalized, Type 4 |
LPD035 |
CGL4 |
| Lipodystrophy, Familial Partial, Type 1 |
LPD040 |
FPLD1 |
| Lipodystrophy, Familial Partial, Type 2 |
LPD015 |
FPLD2 |
| Lipodystrophy, Familial Partial, Type 3 |
LPD021 |
FPLD3 |
| Lipodystrophy, Familial Partial, Type 4 |
LPD034 |
FPLD4 |
| Lipodystrophy, Familial Partial, Type 5 |
LPD030 |
FPLD5 |
| Lipodystrophy, Familial Partial, Type 6 |
LPD036 |
FPLD6 |
| Lipodystrophy, Familial Partial, Type 7 |
LPD044 |
FPLD7 |
| Lipodystrophy, Generalized, with Mental Retardation, Deafness, Short Stature, and Slender Bones |
LPD041 |
|
| Lipodystrophy, Partial, Acquired |
LPD019 |
APLD |
| Lipodystrophy, Partial, Acquired, with Low Complement Component C3, with or Without Glomerulonephritis |
LPD043 |
APLDC3 |
| Lipogranulomatosis |
LPG001 |
|
| Lipoic Acid Biosynthesis Defects |
LPC004 |
|
| Lipoic Acid Synthetase Deficiency |
LPC003 |
|
| Lipoid Congenital Adrenal Hyperplasia |
LPD012 |
LCAH |
| Lipoid Nephrosis |
LPD004 |
MCNS |
| Lipoid Proteinosis of Urbach and Wiethe |
LPD016 |
LIP |
| Lipoma Associated with Neurospinal Dysraphism |
LPM014 |
|
| Lipoma of Colon |
LPM002 |
|
| Lipoma of Spermatic Cord |
LPM001 |
|
| Lipoma of the Conjunctiva |
LPM013 |
|
| Lipoma of the Rectum |
LPM003 |
|
| Lipomatosis |
LPM005 |
|
| Lipomatosis, Multiple |
LPM012 |
FML |
| Lipomatosis, Multiple Symmetric |
LPM010 |
MSL |
| Lipomyelomeningocele |
LPM007 |
|
| Lipoprotein Glomerulopathy |
LPP002 |
LPG |
| Lipoprotein Types--Ld System |
LPP004 |
|
| Lipoprotein Types--Lt System |
LPP005 |
|
| Lipoprotein, Variant of Beta |
LPP006 |
|
| Liposarcoma |
LPS002 |
|
| Liposarcoma of Bone |
LPS001 |
|
| Liposarcoma of the Ovary |
LPS003 |
|
| Lipoyltransferase 1 Deficiency |
LPY002 |
LIPT1D |
| Lissencephaly |
LSS002 |
|
| Lissencephaly 1 |
LSS005 |
LIS1 |
| Lissencephaly 2 |
LSS006 |
LIS2 |
| Lissencephaly 3 |
LSS009 |
LIS3 |
| Lissencephaly 4 |
LSS010 |
LIS4 |
| Lissencephaly 5 |
LSS025 |
LIS5 |
| Lissencephaly 6 with Microcephaly |
LSS039 |
LIS6 |
| Lissencephaly 7 with Cerebellar Hypoplasia |
LSS030 |
LIS7 |
| Lissencephaly 8 |
LSS035 |
LIS8 |
| Lissencephaly 9 with Complex Brainstem Malformation |
LSS040 |
LIS9 |
| Lissencephaly Type 3-Familial Fetal Akinesia Sequence Syndrome |
LSS032 |
|
| Lissencephaly Type Iii and Bone Dysplasia |
LSS034 |
|
| Lissencephaly with Cerebellar Hypoplasia |
LSS024 |
LCH |
| Lissencephaly with Cerebellar Hypoplasia Type a |
LSS021 |
|
| Lissencephaly with Cerebellar Hypoplasia Type B |
LSS020 |
|
| Lissencephaly with Cerebellar Hypoplasia Type C |
LSS023 |
|
| Lissencephaly with Cerebellar Hypoplasia Type D |
LSS022 |
|
| Lissencephaly with Cerebellar Hypoplasia Type E |
LSS019 |
|
| Lissencephaly with Cerebellar Hypoplasia Type F |
LSS018 |
|
| Lissencephaly, Familial, with Cleft Palate and Cerebellar Hypoplasia |
LSS038 |
|
| Lissencephaly, X-Linked, 1 |
LSS036 |
LISX1 |
| Lissencephaly, X-Linked, 2 |
LSS037 |
LISX2 |
| Listeria Meningitis |
LST003 |
|
| Listeriosis |
LST001 |
|
| Lithium Transport |
LTH043 |
|
| Littoral Cell Angioma of the Spleen |
LTT006 |
|
| Littre Gland Carcinoma |
LTT003 |
|
| Livedoid Vasculitis |
LVD003 |
|
| Liver Adenomatosis |
LVR032 |
|
| Liver Angiosarcoma |
LVR002 |
|
| Liver Benign Neoplasm |
LVR031 |
|
| Liver Carcinoma in Situ |
LVR003 |
|
| Liver Cirrhosis |
LVR012 |
CIRRH |
| Liver Disease |
LVR013 |
|
| Liver Failure, Infantile, Transient |
LVR030 |
LFIT |
| Liver Fibrocystic Disease and Polydactyly |
LVR029 |
|
| Liver Fibroma |
LVR007 |
|
| Liver Fibrosarcoma |
LVR008 |
|
| Liver Inflammatory Pseudotumor |
LVR004 |
|
| Liver Leiomyoma |
LVR005 |
|
| Liver Leiomyosarcoma |
LVR010 |
|
| Liver Lipoma |
LVR001 |
|
| Liver Lymphoma |
LVR006 |
|
| Liver Rhabdomyosarcoma |
LVR009 |
|
| Liver Sarcoma |
LVR014 |
|
| Lmna-Related Cardiocutaneous Progeria Syndrome |
LMN005 |
LCPS |
| Lmna-Related Dilated Cardiomyopathy |
LMN001 |
|
| Lobar Holoprosencephaly |
LBR025 |
|
| Lobomycosis |
LBM003 |
|
| Lobular Neoplasia |
LBL001 |
|
| Localized Anterior Staphyloma |
LCL001 |
|
| Localized Chondrosarcoma |
LCL005 |
|
| Localized Hypertrophic Neuropathy |
LCL011 |
|
| Localized Intraductal Papillomatosis |
LCL007 |
|
| Localized Junctional Epidermolysis Bullosa, Non-Herlitz Type |
LCL021 |
|
| Localized Lichen Myxedematosus with Mixed Features of Different Subtypes |
LCL018 |
|
| Localized Lichen Myxedematosus with Monoclonal Gammopathy or Systemic Symptoms |
LCL019 |
|
| Localized Lipodystrophy |
LCL022 |
|
| Localized Osteosarcoma |
LCL004 |
|
| Localized Pagetoid Reticulosis |
LCL017 |
|
| Localized Pulmonary Fibrosis |
LCL003 |
|
| Localized Scleroderma |
LCL006 |
|
| Locked-in Syndrome |
LCK001 |
|
| Loeffler Endocarditis |
LFF001 |
|
| Loeffler Syndrome |
LFF002 |
|
| Loeys-Dietz Syndrome |
LYS001 |
LDS |
| Loeys-Dietz Syndrome 1 |
LYS019 |
LDS1 |
| Loeys-Dietz Syndrome 2 |
LYS018 |
LDS2 |
| Loeys-Dietz Syndrome 3 |
LYS021 |
LDS3 |
| Loeys-Dietz Syndrome 4 |
LYS017 |
LDS4 |
| Loeys-Dietz Syndrome 5 |
LYS020 |
LDS5 |
| Logopenic Progressive Aphasia |
LGP003 |
LPA |
| Loiasis |
LSS001 |
|
| Loin Pain Hematuria Syndrome |
LNP001 |
LPHS |
| Long Bones of Lower Limb Cancer |
LNG027 |
|
| Long Chain Fatty Acids, Defect in Transport of |
LNG107 |
|
| Long Qt Syndrome |
LNG028 |
LQT |
| Long Qt Syndrome 1 |
LNG044 |
LQT1 |
| Long Qt Syndrome 10 |
LNG045 |
LQT10 |
| Long Qt Syndrome 11 |
LNG046 |
LQT11 |
| Long Qt Syndrome 12 |
LNG056 |
LQT12 |
| Long Qt Syndrome 13 |
LNG057 |
LQT13 |
| Long Qt Syndrome 14 |
LNG098 |
LQT14 |
| Long Qt Syndrome 15 |
LNG096 |
LQT15 |
| Long Qt Syndrome 2 |
LNG047 |
LQT2 |
| Long Qt Syndrome 3 |
LNG048 |
LQT3 |
| Long Qt Syndrome 5 |
LNG050 |
LQT5 |
| Long Qt Syndrome 6 |
LNG051 |
LQT6 |
| Long Qt Syndrome 8 |
LNG052 |
LQT8 |
| Long Qt Syndrome 9 |
LNG053 |
LQT9 |
| Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency |
LNG073 |
LCHAD DEFICIENCY |
| Longevity 1 |
LNG066 |
|
| Longevity 2 |
LNG062 |
LGV2 |
| Longitudinal Limb Defect |
LNG112 |
|
| Longitudinal Vaginal Septum |
LNG081 |
|
| Long-Thumb Brachydactyly Syndrome |
LNG102 |
|
| Loose Anagen Hair Syndrome |
LSN002 |
LAHS |
| Lopes-Maciel-Rodan Syndrome |
LPS021 |
LOMARS |
| Louping Ill |
LPN001 |
|
| Louse-Borne Relapsing Fever |
LSB001 |
|
| Low Compliance Bladder |
LWC001 |
|
| Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6 |
LWD006 |
LDLCQ6 |
| Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 7 |
LWD007 |
LDLCQ7 |
| Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 8 |
LWD008 |
LDLCQ8 |
| Low Density Lipoprotein Cholesterol, Mild Elevation of |
LWD005 |
|
| Low Density Lipoprotein, Variation in Molecular Weight of |
LWD004 |
|
| Low Implantation of Placenta |
LWM001 |
|
| Low Isolated Anorectal Malformation |
LWS004 |
|
| Lowe Oculocerebrorenal Syndrome |
LWC002 |
OCRL |
| Lower Clivus Meningioma |
LWR003 |
|
| Lower Gum Cancer |
LWR002 |
|
| Lower Limb Hypertrophy |
LWR014 |
|
| Lower Limb Malformation-Hypospadias Syndrome |
LWR017 |
|
| Lower Lip Cancer |
LWR001 |
|
| Lower Lip Fistula |
LWR011 |
|
| Lower Mesodermal Defects Sequence |
LWR006 |
|
| Lower Urinary Tract Calculus |
LWR004 |
|
| Lower Urinary Tract Obstruction, Congenital |
LWR018 |
LUTO |
| Low-Flow Priapism |
LWF001 |
|
| Low-Grade Astrocytoma |
LWG005 |
|
| Low-Grade Neuroendocrine Tumor of the Corpus Uteri |
LWG004 |
|
| Lowry-Maclean Syndrome |
LWR016 |
|
| Lrp5-Related Primary Osteoporosis |
LRP007 |
|
| Lrrk2 Parkinson Disease |
LRR002 |
|
| Ltbp4-Related Cutis Laxa |
LTB003 |
URDS |
| Lubani-Al Saleh-Teebi Syndrome |
LBN005 |
|
| Lubs X-Linked Mental Retardation Syndrome |
LBS001 |
MRXSL |
| Ludwig's Angina |
LDW001 |
|
| Lujan Syndrome |
LJN002 |
LFS |
| Lujan-Fryns Syndrome |
LJN003 |
LUJFRYS |
| Lujo Hemorrhagic Fever |
LJH001 |
|
| Lumbar Plexus Neoplasm |
LMB005 |
|
| Lumbar Spinal Canal and Spinal Cord Meningioma |
LMB007 |
|
| Lumbar Stenosis, Familial |
LMB070 |
|
| Lumbar Syndrome |
LMB076 |
|
| Lumbosacral Lipoma |
LMB003 |
|
| Lumbosacral Plexus Lesion |
LMB001 |
|
| Lumbosacral Spina Bifida Aperta |
LMB057 |
|
| Lumbosacral Spina Bifida Cystica |
LMB056 |
|
| Luminal Breast Carcinoma |
LMN006 |
|
| Lung Abscess |
LNG095 |
|
| Lung Acinar Adenocarcinoma |
LNG022 |
|
| Lung Adenoid Cystic Carcinoma |
LNG011 |
|
| Lung Adenoma |
LNG030 |
|
| Lung Agenesis, Congenital Heart Defects, and Thumb Anomalies Syndrome |
LNG101 |
LACHT |
| Lung Benign Neoplasm |
LNG031 |
|
| Lung Cancer |
LNG032 |
LNCR |
| Lung Cancer Susceptibility 1 |
LNG109 |
LNCR1 |
| Lung Cancer Susceptibility 3 |
LNG064 |
LNCR3 |
| Lung Cancer Susceptibility 4 |
LNG065 |
LNCR4 |
| Lung Cancer Susceptibility 5 |
LNG086 |
LNCR5 |
| Lung Carcinoma in Situ |
LNG003 |
|
| Lung Clear Cell Carcinoma |
LNG001 |
|
| Lung Clear Cell-Sugar-Tumor |
LNG010 |
|
| Lung Combined Large Cell Neuroendocrine Carcinoma |
LNG002 |
|
| Lung Combined Type Small Cell Adenocarcinoma |
LNG090 |
|
| Lung Combined Type Small Cell Carcinoma |
LNG019 |
|
| Lung Disease |
LNG099 |
|
| Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome |
LNG105 |
LICS |
| Lung Giant Cell Carcinoma |
LNG017 |
|
| Lung Hilum Cancer |
LNG034 |
|
| Lung Large Cell Carcinoma |
LNG035 |
|
| Lung Leiomyoma |
LNG036 |
|
| Lung Leiomyosarcoma |
LNG023 |
|
| Lung Lymphoma |
LNG013 |
|
| Lung Meningioma |
LNG009 |
|
| Lung Mixed Small Cell and Squamous Cell Carcinoma |
LNG007 |
|
| Lung Mucinous Cystadenocarcinoma |
LNG110 |
|
| Lung Mucoepidermoid Carcinoma |
LNG091 |
|
| Lung Non-Squamous Non-Small Cell Carcinoma |
LNG111 |
|
| Lung Oat Cell Carcinoma |
LNG020 |
|
| Lung Occult Adenocarcinoma |
LNG005 |
|
| Lung Occult Large Cell Carcinoma |
LNG006 |
|
| Lung Occult Small Cell Carcinoma |
LNG021 |
|
| Lung Occult Squamous Cell Carcinoma |
LNG012 |
|
| Lung Papillary Adenocarcinoma |
LNG016 |
|
| Lung Sarcoma |
LNG037 |
|
| Lung Squamous Cell Carcinoma |
LNG039 |
|
| Lung Superior Sulcus Carcinoma |
LNG014 |
|
| Lunulae of Fingernails |
LNL001 |
|
| Lupus - Neurological Sequelae |
LPS008 |
|
| Lupus Erythematosus |
LPS004 |
SLE |
| Lupus Erythematosus Panniculitis |
LPS018 |
|
| Lupus Erythematosus Tumidus |
LPS019 |
|
| Luscan-Lumish Syndrome |
LSC003 |
LLS |
| Lutembacher's Syndrome |
LTM001 |
|
| Luteoma |
LTM002 |
|
| Lutheran Null |
LTH044 |
|
| Luxation of Globe |
LXT001 |
|
| Lyme Disease |
LYM017 |
LYM |
| Lyme Disease - Neurological Complications |
LYM055 |
|
| Lymph Node Adenoid Cystic Carcinoma |
LYM108 |
|
| Lymph Node Cancer |
LYM020 |
|
| Lymph Node Disease |
LYM116 |
|
| Lymph Node Palisaded Myofibroblastoma |
LYM016 |
|
| Lymph Node Tuberculosis |
LYM010 |
|
| Lymphadenitis |
LYM021 |
|
| Lymphangiectasia, Intestinal |
LYM124 |
|
| Lymphangiectasia, Pulmonary, Congenital |
LYM122 |
CPL |
| Lymphangiectasis |
LYM035 |
|
| Lymphangioleiomyomatosis |
LYM007 |
LAM |
| Lymphangioma |
LYM022 |
|
| Lymphangiomatosis |
LYM095 |
|
| Lymphangiosarcoma |
LYM008 |
|
| Lymphangitis |
LYM014 |
|
| Lymphatic Malformation 1 |
LYM144 |
LMPHM1 |
| Lymphatic Malformation 2 |
LYM146 |
LMPHM2 |
| Lymphatic Malformation 3 |
LYM147 |
LMPHM3 |
| Lymphatic Malformation 4 |
LYM148 |
LMPHM4 |
| Lymphatic Malformation 5 |
LYM145 |
LMPHM5 |
| Lymphatic Malformation 6 |
LYM149 |
LMPHM6 |
| Lymphatic Malformation 7 |
LYM150 |
LMPHM7 |
| Lymphatic System Cancer |
LYM023 |
|
| Lymphatic System Disease |
LYM024 |
|
| Lymphedema |
LYM025 |
|
| Lymphedema and Cerebral Arteriovenous Anomaly |
LYM037 |
|
| Lymphedema, Cardiac Septal Defects, and Characteristic Facies |
LYM125 |
|
| Lymphedema, Primary, with Myelodysplasia |
LYM094 |
LMPM |
| Lymphedema-Distichiasis Syndrome |
LYM029 |
LPHDST |
| Lymphedema-Hypoparathyroidism Syndrome |
LYM123 |
|
| Lymphoblastic Leukemia, Acute, with Lymphomatous Features |
LYM138 |
LALL |
| Lymphoblastic Lymphoma |
LYM040 |
|
| Lymphoblastic Transformation, Inhibition of |
LYM134 |
|
| Lymphoblastic Transformation, Intrinsic Defect in |
LYM136 |
|
| Lymphocele |
LYM005 |
|
| Lymphocyte Cytosol Polypeptide, 40-Kd |
LYM131 |
LCP40 |
| Lymphocyte Cytosol Polypeptide, 49-Kd |
LYM132 |
LCP49 |
| Lymphocytic Choriomeningitis |
LYM009 |
LCM |
| Lymphocytic Colitis |
LYM042 |
|
| Lymphocytic Gastritis |
LYM015 |
|
| Lymphocytic Hypereosinophilic Syndrome |
LYM117 |
HES-L |
| Lymphocytic Hypophysitis |
LYM043 |
LH |
| Lymphocytic Infiltrate of Jessner |
LYM044 |
|
| Lymphocytic Leukemia |
LYM031 |
|
| Lymphoepithelial-Like Carcinoma |
LYM100 |
|
| Lymphoepithelioma-Like Acinar Prostate Adenocarcinoma |
LYM003 |
|
| Lymphoepithelioma-Like Carcinoma |
LYM006 |
|
| Lymphoepithelioma-Like Thymic Carcinoma |
LYM018 |
|
| Lymphogranuloma Venereum |
LYM011 |
LGV |
| Lymphohistiocytoid Mesothelioma |
LYM001 |
|
| Lymphoid Hemopathy |
LYM152 |
|
| Lymphoid Interstitial Pneumonia |
LYM004 |
LIP |
| Lymphoid System Deterioration, Progressive |
LYM137 |
|
| Lymphokine Deficiency |
LYM139 |
|
| Lymphoma |
LYM118 |
|
| Lymphoma Aids Related |
LYM126 |
PEL |
| Lymphoma, Hodgkin, Classic |
LYM133 |
CHL |
| Lymphoma, Hodgkin, X-Linked Pseudoautosomal |
LYM141 |
|
| Lymphoma, Hodgkin, Y-Linked Pseudoautosomal |
LYM142 |
|
| Lymphoma, Large-Cell, Immunoblastic |
LYM048 |
|
| Lymphoma, Mucosa-Associated Lymphoid Type |
LYM129 |
MALTOMA |
| Lymphoma, Non-Hodgkin, Familial |
LYM143 |
NHL |
| Lymphoma-Like Variant Infiltrating Bladder Urothelial Carcinoma |
LYM013 |
|
| Lymphomatoid Granulomatosis |
LYM051 |
LYG |
| Lymphomatoid Papulosis |
LYM052 |
LYP |
| Lymphomatous Thyroiditis |
LYM053 |
|
| Lymphopenia |
LYM027 |
|
| Lymphopenic Hypergammaglobulinemia, Antibody Deficiency, Autoimmune Hemolytic Anemia, and Glomerulonephritis |
LYM140 |
|
| Lymphoplasmacyte-Rich Meningioma |
LYM002 |
|
| Lymphoplasmacytic Inflammatory Pseudotumor of the Liver |
LYM153 |
|
| Lymphoplasmacytic Lymphoma |
LYM012 |
WM |
| Lymphoplasmacytic Lymphoma Without Igm Production |
LYM119 |
|
| Lymphoproliferative Disease Associated with Primary Immune Disease |
LYM154 |
|
| Lymphoproliferative Syndrome |
LYM033 |
|
| Lymphoproliferative Syndrome 1 |
LYM106 |
LPFS1 |
| Lymphoproliferative Syndrome 2 |
LYM107 |
LPFS2 |
| Lymphoproliferative Syndrome 3 |
LYM151 |
LPFS3 |
| Lymphoproliferative Syndrome, X-Linked, 1 |
LYM113 |
XLP1 |
| Lymphoproliferative Syndrome, X-Linked, 2 |
LYM114 |
XLP2 |
| Lymphosarcoma |
LYM019 |
|
| Lynch Syndrome |
LYN001 |
COCA1 |
| Lynch Syndrome I |
LYN004 |
HNPCC1 |
| Lysine Malabsorption Syndrome |
LYS022 |
|
| Lysinuric Protein Intolerance |
LYS003 |
LPI |
| Lysosomal Acid Lipase Deficiency |
LYS012 |
CESD |
| Lysosomal and Lipase Deficiency |
LYS024 |
|
| Lysosomal Disease |
LYS029 |
|
| Lysosomal Disease with Epilepsy |
LYS027 |
|
| Lysosomal Disease with Hypertrophic Cardiomyopathy |
LYS025 |
|
| Lysosomal Disease with Restrictive Cardiomyopathy |
LYS026 |
|
| Lysosomal Glycogen Storage Disease |
LYS028 |
|
| Lysosomal Storage Disease |
LYS002 |
|
| Lysosomal Storage Disease with Skeletal Involvement |
LYS030 |
|
