| 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
|
| 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
|
| Langer Nishino Yamaguchi Syndrome
|
LNG042
|
|
| Langerhans Cell Histiocytosis
|
LNG108
|
LCH
|
| Langerhans Cell Histiocytosis in Childhood and Adulthood
|
LNG083
|
|
| Langerhans Cell Histiocytosis Specific to Adulthood
|
LNG085
|
|
| Langerhans Cell Histiocytosis Specific to Childhood
|
LNG084
|
|
| 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 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 Cancer, Childhood
|
LRY025
|
|
| 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 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 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
|
| 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
|
|
| 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 Short-Limb Skeletal Dysplasia, Al Gazali Type
|
LTH046
|
|
| Letrozole Toxicity
|
LTR016
|
|
| Letterer-Siwe Disease
|
LTT002
|
LESD
|
| Leucocyte Adhesion Defect
|
LCC001
|
|
| 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, B-Cell, Chronic
|
LKM004
|
|
| 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
|
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, 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
|
| Leukodystrophy, Pseudometachromatic
|
LKD006
|
|
| Leukoencephalopathy Palmoplantar Keratoderma
|
LKN004
|
|
| Leukoencephalopathy with Ataxia
|
LKN017
|
LKPAT
|
| Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation
|
LKN026
|
LBSL
|
| Leukoencephalopathy with Calcifications and Cysts
|
LKN028
|
LCC
|
| Leukoencephalopathy with Dystonia and Motor Neuropathy
|
LKN010
|
LKDMN
|
| Leukoencephalopathy with Metaphyseal Chondrodysplasia
|
LKN009
|
LKMCD
|
| 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
|
| Leukoencephalopathy-Spondylometaphyseal Dysplasia Syndrome
|
LKN029
|
H-SMD
|
| Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis
|
LKM069
|
|
| Leukonychia Totalis
|
LKN007
|
NDNC3
|
| 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
|
|
| Levy-Yeboa Syndrome
|
LVY001
|
|
| 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
|
| Lice Infestation
|
LCN001
|
|
| Lichen Amyloidosis
|
LCH014
|
|
| Lichen Disease
|
LCH004
|
|
| Lichen Nitidus
|
LCH003
|
|
| Lichen Planopilaris
|
LCH011
|
LPP
|
| Lichen Planus
|
LCH002
|
|
| Lichen Planus Pemphigoides
|
LCH013
|
|
| Lichen Planus Pigmentosus
|
LCH008
|
|
| Lichen Planus, Familial
|
LCH017
|
|
| Lichen Sclerosus
|
LCH009
|
|
| 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 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
|
| Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy
|
LPT011
|
|
| Lipoblastoma
|
LPB001
|
|
| Lipodermatosclerosis
|
LPD014
|
|
| Lipodystrophy Due to Peptidic Growth Factors Deficiency
|
LPD028
|
|
| 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 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 Gorlin Syndrome
|
LPS006
|
|
| 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
|
|
| Low-Flow Priapism
|
LWF001
|
|
| Low-Grade Astrocytoma
|
LWG005
|
|
| Low-Grade Neuroendocrine Tumor of the Corpus Uteri
|
LWG004
|
|
| Lowry-Maclean Syndrome
|
LWR016
|
|
| Lrba Deficiency
|
LRB003
|
|
| Lrp5-Related Primary Osteoporosis
|
LRP007
|
|
| Lrrk2-Related Parkinson Disease
|
LRR001
|
PARK8
|
| Ltbp4-Related Cutis Laxa
|
LTB003
|
URDS
|
| Lubani-Al Saleh-Teebi Syndrome
|
LBN005
|
|
| Lubinsky Syndrome
|
LBN003
|
|
| 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 Malformations
|
LYM127
|
|
| 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
|
|
| Lymphoadenopathic Mastocytosis with Eosinophilia
|
LYM096
|
|
| 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
|
|
| Lymphocytic Vasculitis
|
LYM045
|
|
| 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
|
|
| 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 Meningitis
|
LYM098
|
|
| 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
|
|
