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
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