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 Muscular Dystrophy |
LM2002 |
|
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 |
|
Laron Syndrome |
LRN002 |
LARS |
Laron Syndrome with Immunodeficiency |
LRN007 |
|
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 |
|
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 Alzheimer Disease |
LTN003 |
|
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 Sy |
LTN031 |
|
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 |
|
Late-Onset Steinert Myotonic Dystrophy |
LTN030 |
|
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 |
PLS |
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 |
LATHOS |
Lathyrism |
LTH004 |
|
Lattice Corneal Dystrophy |
LTT001 |
|
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 |
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 / 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 Hereditary Optic Neuropathy with Demyelinating Disease of Cns |
LBR037 |
|
Leber Hereditary Optic Neuropathy, Autosomal Recessive |
LBR039 |
LHONAR |
Leber Hereditary Optic Neuropathy, Modifier of |
LBR038 |
LOAM |
Leber Optic Atrophy and Dystonia |
LBR031 |
LDYT |
Leber Plus Disease |
LBR036 |
CRB |
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 |
|
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 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-Kreienkamp Syndrome |
LSS043 |
LESKRES |
Lessel-Kubisch Syndrome |
LSS041 |
LSKB |
Lethal Brain and Heart Developmental Defects |
LTH051 |
|
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 |
|
Lethal Multiple Congenital Anomalies/dysmorphic Syndrome |
LTH049 |
|
Lethal Neonatal Spasticity-Epileptic Encephalopathy Syndrome |
LTH036 |
|
Lethal Recessive Chondrodysplasia |
LTH052 |
|
Lethal Restrictive Dermopathy |
LTH053 |
|
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 |
Leukemia, T-Cell, Chronic |
LKM005 |
|
Leukocoria |
LKC002 |
|
Leukocyte Adhesion Deficiency, Type I |
LKC009 |
LAD1 |
Leukocyte Adhesion Deficiency, Type Iii |
LKC005 |
LAD3 |
Leukocyte Disease |
LKC003 |
|
Leukocyte Nuclear Appendages, Hereditary Prevalence of |
LKC010 |
|
Leukodystrophy |
LKD001 |
|
Leukodystrophy and Acquired Microcephaly with or Without Dystonia |
LKD024 |
LDAMD |
Leukodystrophy, Childhood-Onset, Remitting |
LKD038 |
CORLK |
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, 20 |
LKD033 |
HLD20 |
Leukodystrophy, Hypomyelinating, 21 |
LKD034 |
HLD21 |
Leukodystrophy, Hypomyelinating, 22 |
LKD035 |
HLD22 |
Leukodystrophy, Hypomyelinating, 23, with Ataxia, Deafness, Liver Dysfunction, and Dilated Cardiomyopathy |
LKD036 |
HLD23 |
Leukodystrophy, Hypomyelinating, 24 |
LKD037 |
HLD24 |
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, Developmental Delay, and Episodic Neurologic Regression Syndrome |
LKN030 |
LEUDEN |
Leukoencephalopathy, Hereditary Diffuse, with Spheroids 1 |
LKN033 |
HDLS1 |
Leukoencephalopathy, Hereditary Diffuse, with Spheroids 2 |
LKN034 |
HDLS2 |
Leukoencephalopathy, Motor Delay, Spasticity, and Dysarthria Syndrome |
LKN031 |
LEMSPAD |
Leukoencephalopathy, Progressive, Infantile-Onset, with or Without Deafness |
LKN032 |
LEPID |
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 |
|
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 Ii |
LYD013 |
|
Leydig Cell Hypoplasia, Type I |
LYD012 |
LHR |
Leydig Cell Tumor |
LYD001 |
|
L-Ferritin Deficiency |
LFR008 |
LFTD |
Liang-Wang Syndrome |
LNG113 |
LIWAS |
Liberfarb Syndrome |
LBR035 |
LIBF |
Libman-Sacks Endocarditis |
LBM007 |
|
Li-Campeau Syndrome |
LCM001 |
LICAS |
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 |
Li-Ghorbani-Weisz-Hubshman Syndrome |
LGH020 |
LIGOWS |
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 |
|
Limbic Encephalitis |
LMB024 |
|
Limbic Encephalitis with Lgi1 Antibodies |
LMB053 |
|
Limb-Mammary Syndrome |
LMB008 |
LMS |
Limited Scleroderma |
LMT001 |
|
Linear Atrophoderma of Moulin |
LNR009 |
|
Linear Focal Elastosis |
LNR017 |
|
Linear Hamartoma Syndrome |
LNR002 |
|
Linear Hypopigmentation and Craniofacial Asymmetry with Acral, Ocular and Brain Anomalies |
LNR018 |
|
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 Leukomelanoder |
LPT015 |
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 |
Lipofibromatosis-Like Neural Tumor |
LPF001 |
|
Lipogranulomatosis |
LPG001 |
|
Lipoic Acid Biosynthesis Defects |
LPC004 |
|
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 Quantitative Trait Locus |
LPP008 |
LPAQTL |
Lipoprotein Glomerulopathy |
LPP002 |
LPG |
Lipoprotein Types--Ld System |
LPP004 |
|
Liposarcoma |
LPS002 |
|
Liposarcoma of Bone |
LPS001 |
|
Liposarcoma of the Ovary |
LPS003 |
|
Lipoyltransferase 1 Deficiency |
LPY002 |
LIPT1D |
Lissencephaly |
LSS002 |
|
Lissencephaly 1 |
LSS005 |
LIS1 |
Lissencephaly 10 |
LSS042 |
LIS10 |
Lissencephaly 2 |
LSS006 |
LIS2 |
Lissencephaly 3 |
LSS009 |
LIS3 |
Lissencephaly 4 |
LSS010 |
LIS4 |
Lissencephaly 5 |
LSS025 |
LIS5 |
Lissencephaly 6 |
LSS044 |
LIS6 |
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 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 Disease, Severe Congenital |
LVR033 |
SCOLIV |
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 |
|
Lmnb1-Related Autosomal Dominant Leukodystrophy |
LMN017 |
|
Lobar Holoprosencephaly |
LBR025 |
|
Lobomycosis |
LBM003 |
|
Lobular Neoplasia |
LBL001 |
|
Localized Anterior Staphyloma |
LCL001 |
|
Localized Chondrosarcoma |
LCL005 |
|
Localized Dystrophic Epidermolysis Bullosa |
LCL023 |
|
Localized Dystrophic Epidermolysis Bullosa, Acral Form |
LCL025 |
|
Localized Dystrophic Epidermolysis Bullosa, Nails Only |
LCL024 |
|
Localized Hypertrophic Neuropathy |
LCL011 |
|
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 |
Loeys-Dietz Syndrome 6 |
LYS031 |
LDS6 |
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 Covid |
LNG116 |
PASC |
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 16 |
LNG114 |
LQT16 |
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 |
Long-Chain Hydroxyacyl-Coa Dehydrogenase Deficiency / Trifunctional Protein Deficiency |
LNG118 |
|
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 Grade Glioma |
LWG006 |
|
Low Implantation of Placenta |
LWM001 |
|
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 |
|
Lowry-Wood Syndrome |
LWR019 |
LWS |
Lrba Deficiency |
LRB003 |
|
Lrp5-Related Primary Osteoporosis |
LRP007 |
|
Lrrk2 Parkinson Disease |
LRR002 |
|
Ltbp4-Related Cutis Laxa |
LTB003 |
URDS |
Lubani-Al Saleh-Teebi Syndrome |
LBN005 |
|
Ludwig's Angina |
LDW001 |
|
Lujan Syndrome |
LJN002 |
LFS |
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 a |
LMN015 |
|
Luminal Breast Carcinoma B |
LMN016 |
|
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 Pleomorphic Carcinoma |
LNG117 |
|
Lung Sarcoma |
LNG037 |
|
Lung Sarcomatoid Carcinoma |
LNG115 |
|
Lung Squamous Cell Carcinoma |
LNG039 |
|
Lung Superior Sulcus Carcinoma |
LNG014 |
|
Lunulae of Fingernails |
LNL001 |
|
Luo-Schoch-Yamamoto Syndrome |
LSC005 |
LUSYAM |
Lupus Erythematosus |
LPS004 |
LUPUS |
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 |
Lymph Node Adenoid Cystic Carcinoma |
LYM108 |
|
Lymph Node Benign Neoplasm |
LYM156 |
|
Lymph Node Carcinoma |
LYM157 |
|
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 10 |
LYM159 |
LMPHM10 |
Lymphatic Malformation 11 |
LYM160 |
LMPHM11 |
Lymphatic Malformation 12 |
LYM161 |
LMPHM12 |
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 Malformation 8 |
LYM155 |
LMPHM8 |
Lymphatic Malformation 9 |
LYM158 |
LMPHM9 |
Lymphatic System Cancer |
LYM023 |
|
Lymphatic System Disease |
LYM024 |
|
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 |
|
Lymphocytic Choriomeningitis |
LYM009 |
LCM |
Lymphocytic Colitis |
LYM042 |
|
Lymphocytic Gastritis |
LYM015 |
|
Lymphocytic Hypereosinophilic Syndrome |
LYM117 |
HES-L |
Lymphocytic Hypophysitis |
LYM043 |
|
Lymphocytic Infiltrate of Jessner |
LYM044 |
|
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 |
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 |
|
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 |
HNPCC |
Lynch Syndrome 1 |
LYN005 |
LYNCH1 |
Lynch Syndrome 2 |
LYN006 |
LYNCH2 |
Lynch Syndrome 4 |
LYN008 |
LYNCH4 |
Lynch Syndrome 5 |
LYN009 |
LYNCH5 |
Lynch Syndrome 8 |
LYN007 |
LYNCH8 |
Lysine Malabsorption Syndrome |
LYS022 |
|
Lysinuric Protein Intolerance |
LYS003 |
LPI |
Lysis by Alloreactive Natural Killer Cells |
LYS023 |
EC1 |
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 |
|