- Lichen amyloidosis familial - See Primary cutaneous amyloidosis
- Lichen follicularis - See Lichen planopilaris
- Lichen myxedematosus - See Papular mucinosis
- Lichen myxoedematosus - See Papular mucinosis
- Lichen planopilaris
- Lichen planopilaris classic type - See Lichen planopilaris
- Lichen planus actinus - See Actinic lichen planus
- Lichen planus follicularis - See Lichen planopilaris
- Lichen planus pemphigoides
- Lichen planus pigmentosa - See Lichen planus pigmentosus
- Lichen planus pigmentosus
- Lichen planus pigmentosus inversus - See Lichen planus pigmentosus
- Lichen planus subtropicus - See Actinic lichen planus
- Lichen planus tropicus - See Actinic lichen planus
- Lichen sclerosis - See Lichen sclerosus
- Lichen sclerosis et atrophicus - See Lichen sclerosus
- Lichen sclerosus
- Lichen sclerosus et atrophicus - See Lichen sclerosus
- Lichenoid melanodermatitis - See Actinic lichen planus
- Lichtenstein syndrome
- Liddle syndrome
- Liddle's syndrome - See Liddle syndrome
- Liebenberg syndrome - See Brachydactyly elbow wrist dysplasia
- Li-Fraumeni syndrome
- Light chain amyloidosis - See AL amyloidosis
- Light chain deposition disease
- Light-chain deposition disease - See Light chain deposition disease
- Ligneous conjunctivitis
- Limb body wall complex - See Limb-body wall complex
- Limb deficiencies distal with micrognathia
- Limb deficiency-heart malformation syndrome - See Fibular aplasia, tibial campomelia, and oligosyndactyly syndrome
- Limb girdle muscular dystrophy - See Limb-girdle muscular dystrophy
- Limb reduction defect
- Limb scalp and skull defects - See Adams-Oliver syndrome
- Limb uterus syndrome - See Hypomelia mullerian duct anomalies
- Limb, scalp and skull defects - See Adams-Oliver syndrome
- Limb-body wall complex
- Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy - intellectual disability - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy due to caveolin-3 deficiency - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy due to FKRP deficiency - See Limb-girdle muscular dystrophy type 2I
- Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency - See Limb-girdle muscular dystrophy, type 2C
- Limb-girdle muscular dystrophy type 1A
- Limb-girdle muscular dystrophy type 1B
- Limb-girdle muscular dystrophy type 1C - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 1D - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 1E - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 1F - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 1G - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 1H - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2 - See Limb-girdle muscular dystrophy type 2A
- Limb-girdle muscular dystrophy type 2A
- Limb-girdle muscular dystrophy type 2B
- Limb-girdle muscular dystrophy type 2E
- Limb-girdle muscular dystrophy type 2F
- Limb-girdle muscular dystrophy type 2H
- Limb-girdle muscular dystrophy type 2I
- Limb-girdle muscular dystrophy type 2J - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2K - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2L - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2M - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2N - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2O - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2P - See Limb-girdle muscular dystrophy type 1A
- Limb-girdle muscular dystrophy type 2Q - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2S - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy type 2T - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency - See Limb-girdle muscular dystrophy, type 2C
- Limb-girdle muscular dystrophy with Paget disease of bone - See Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
- Limb-girdle muscular dystrophy, type 1G - See Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy, type 2C
- Limb-girdle muscular dystrophy, type 2D
- Limb-girdle muscular dystrophy, type 2G
- Limb-girdle muscular dystrophy-intellectual disability syndrome - See Limb-girdle muscular dystrophy
- Limbic encephalitis
- Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies - See Limbic encephalitis with LGI1 antibodies
- Limbic encephalitis with LGI1 antibodies
- Limb-mammary syndrome
- Limit dextrinosis - See Glycogen storage disease type 3
- Limited cutaneous systemic scleroderma - See Limited cutaneous systemic sclerosis
- Limited cutaneous systemic sclerosis
- Limited systemic sclerosis
- Linear and whorled hypermelanosis - See Linear and whorled nevoid hypermelanosis
- Linear and whorled nevoid hypermelanosis
- Linear hamartoma syndrome
- Linear IgA bullous dermatosis - See Linear IgA disease
- Linear IgA dermatosis - See Linear IgA disease
- Linear IgA disease
- Linear immunoglobulin A (IgA) dermatosis - See Linear IgA disease
- Linear lichen planus
- Linear LP - See Linear lichen planus
- Linear nevus sebaceous syndrome
- Linear porokeratosis
- Linear scleroderma
- Linear skin atrophy, scarring alopecia, anonychia, and tongue lesion - See Sequeiros Sack syndrome
- Linear skin defects with multiple congenital anomalies 1 - See Microphthalmia with linear skin defects syndrome
- Linear verrucose epidermal nevus - See Inflammatory linear verrucous epidermal nevus
- Lin-Gettig syndrome
- Lingua villosa - See Black hairy tongue - not a rare disease
- Linguofacial dyskinesia - See Tardive dyskinesia - not a rare disease
- Lip and oral cavity cancer
- Lip pit syndrome - See Van der Woude syndrome
- Lip pseudocleft-hemangiomatous branchial cyst syndrome - See Branchiooculofacial syndrome
- LIPA deficiency - See Lysosomal acid lipase deficiency
- Lipase D deficiency - See Familial lipoprotein lipase deficiency
- Lipase deficiency combined
- LIPC Deficiency - See Hepatic lipase deficiency
- LIPD deficiency - See Familial lipoprotein lipase deficiency
- Lipedema - not a rare disease
- Lipedematous Scalp
- LIPE-related familial partial lipodystrophy - See Familial partial lipodystrophy
- LIPE-related FPLD - See Familial partial lipodystrophy
- Lipid transport defect of intestine - See Chylomicron retention disease
- Lipidosis with triglycerid storage disease
- Lipid-storage myopathy secondary to short-chain acyl-CoA dehydrogenase deficiency - See Short-chain acyl-CoA dehydrogenase deficiency
- Lipoate biosynthesis defect - See Lipoic acid biosynthesis defects
- Lipoatrophic diabetes - See Familial partial lipodystrophy type 2
- Lipoatrophic diabetes - See Congenital generalized lipodystrophy
- Lipoatrophy with diabetes, hepatic steatosis, cardiomyopathy, and leukomelanodermic papules
- Lipoblastoma
- Lipodermatosclerosis
- Lipodystophy partial progressive - See Barraquer-Simons syndrome
- Lipodystrophy cephalothoracic type - See Barraquer-Simons syndrome
- Lipodystrophy due to peptidic growth factors deficiency
- Lipodystrophy partial acquired - See Barraquer-Simons syndrome
- Lipodystrophy, Berardinelli-Seip congenital, type 4, with muscular dystrophy - See Congenital generalized lipodystrophy type 4
- Lipodystrophy, congenital generalized, type 4 - See Congenital generalized lipodystrophy type 4
- LIPODYSTROPHY, FAMILIAL PARTIAL, ASSOCIATED WITH PPARG MUTATIONS - See Familial partial lipodystrophy associated with PPARG mutations
- Lipodystrophy, familial partial, Dunnigan type - See Familial partial lipodystrophy type 2
- Lipodystrophy, familial partial, type 2 - See Familial partial lipodystrophy type 2
- Lipodystrophy, familial partial, type 4 - See Familial partial lipodystrophy
- Lipodystrophy, familial partial, type 5 - See Familial partial lipodystrophy
- Lipodystrophy, familial partial, type 6 - See Familial partial lipodystrophy
- Lipodystrophy, familial, of limbs and lower trunk - See Familial partial lipodystrophy type 2
- Lipodystrophy, reverse partial - See Familial partial lipodystrophy type 2
- Lipodystrophy, type A, associated with mandibuloacral dysplasia - See Mandibuloacral dysplasia with type A lipodystrophy
- Lipodystrophy, type B, associated with mandibuloacral dysplasia - See Mandibuloacral dysplasia with type B lipodystrophy
- Lipofuscin storage disease - See Ceroid storage disease
- Lipogranulomatosis
- Lipoic acid biosynthesis defect - See Lipoic acid biosynthesis defects
- Lipoic acid biosynthesis defects
- Lipoic acid synthetase deficiency
- Lipoid CAH - See Congenital lipoid adrenal hyperplasia
- Lipoid congenital adrenal hyperplasia - See Congenital lipoid adrenal hyperplasia
- Lipoid granulomatosis - See Erdheim-Chester disease
- Lipoid proteinosis of Urbach and Wiethe
- Lipomatosis of pancreas, congenital - See Shwachman-Diamond syndrome
- Lipomatous medulloblastoma (formerly) - See Cerebellar liponeurocytoma
- Lipomucopolysaccharidosis - See Sialidosis, type II
- Lipomyelomeningocele
- Lipoprotein lipase deficiency - See Familial lipoprotein lipase deficiency
- Lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency - See Lipase deficiency combined
- Lipoprotein lipase deficiency, familial - See Familial lipoprotein lipase deficiency
- Lipoproteinosis - See Lipoid proteinosis of Urbach and Wiethe
- Liposarcoma
- Liposclerotic mesenteritis - See Sclerosing mesenteritis
- Liposomal Acid Lipase Deficiency, Wolman Type - See Wolman disease
- LIS1 - See Lissencephaly 1
- LIS2 - See Lissencephaly 2
- Lison syndrome - See Spastic paraplegia 23
- Lissencephaly
- Lissencephaly 1
- Lissencephaly 2
- Lissencephaly and agenesis of corpus callosum - See Lissencephaly X-linked
- Lissencephaly classic - See Lissencephaly 1
- Lissencephaly sequence isolated - See Lissencephaly 1
- Lissencephaly syndrome Norman-Roberts type - See Lissencephaly 2
- Lissencephaly type 2 with muscular and ocular involvement - Another name for Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
- Lissencephaly X-linked
- Lissencephaly, X-linked 2 - See X-linked lissencephaly with abnormal genitalia
- LISSENCEPHALY, X-LINKED, WITH AMBIGUOUS GENITALIA - See X-linked lissencephaly with abnormal genitalia
- Listeria infection
- Listeria monocytogenes infection - See Listeria infection
- Listeriosis - See Listeria infection
- LISX - See Lissencephaly X-linked
- Littoral cell angioma - See Littoral cell angioma of the spleen
- Littoral cell angioma of the spleen
- Livedo racemosa and cerebrovascular accidents - See Sneddon syndrome
- Livedo racemosa-cerebrovascular accident syndrome - See Sneddon syndrome
- Livedo reticularis and cerebrovascular accidents - See Sneddon syndrome
- Livedo reticularis with summer ulcerations - See Livedoid vasculopathy
- Livedo reticularis with winter ulcerations - See Livedoid vasculopathy
- Livedo reticularis-cerebrovascular accident syndrome - See Sneddon syndrome
- Livedo vasculitis - See Livedoid vasculopathy
- Livedoid vasculitis - See Livedoid vasculopathy
- Livedoid vasculopathy
- Liver glycogen storage disease 0 - See Glycogen storage disease type 0, liver
- Liver glycogen synthase deficiency - See Glycogen storage disease type 0, liver
- Liver GSD 0 - See Glycogen storage disease type 0, liver
- LKS - See Landau-Kleffner syndrome
- LLP - See Linear lichen planus
- L-lysine NAD-oxido-reductase deficiency - See Hyperlysinemia
- LMM - See Lentigo maligna melanoma
- LMNA-related congenital muscular dystrophy - See Congenital muscular dystrophy
- LMPS - See Multiple pterygium syndrome lethal type
- LMS - See Limb-mammary syndrome
- LMS - See Lateral meningocele syndrome
- LNMS - See Laurence-Moon syndrome
- LNS - See Lesch Nyhan syndrome
- Loa loa filariasis - See Loiasis
- Lobar atrophy of the brain - See Pick's disease
- Lobo disease - See Paracoccidioidomycosis
- Lobstein disease - See Osteogenesis imperfecta
- Lobular capillary hemangioma - See Pyogenic granuloma - not a rare disease
- LOCAH - See Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency - not a rare disease
- Local hypoplastic amelogenesis imperfecta - See Amelogenesis imperfecta local hypoplastic
- Localized Castleman disease - See Unicentric Castleman disease
- Localized cicatricial pemphigoid - See Brunsting-Perry syndrome
- Localized deciduous skin - See Acral peeling skin syndrome
- Localized fibrosing scleroderma - See Localized scleroderma
- Localized hypertrophic neuropathy
- Localized junctional epidermolysis bullosa, non-Herlitz type - See Junctional epidermolysis bullosa
- Localized lichen myxedematosus - See Papular mucinosis
- Localized lipodystrophy
- Localized lipodystrophy - See Localized lipodystrophy
- Localized lipomatosis of the scalp with or without alopecia - See Lipedematous Scalp
- Localized pigmented villonodular synovitis - See Pigmented villonodular synovitis
- Localized PSS - See Acral peeling skin syndrome
- Localized pustular psoriasis - See Pustulosis palmaris et plantaris
- Localized scleroderma
- Locked in syndrome - See Locked-in syndrome
- Locked-in syndrome
- Lockjaw - See Tetanus
- Lockwood Feingold syndrome
- LOCS - See Epidermolysis bullosa
- Loeffler syndrome - See Pneumonia, eosinophilic
- Loeys-Dietz aortic aneurysm syndrome - See Loeys-Dietz syndrome
- Loeys-Dietz syndrome
- Loeys-Dietz syndrome 1 - See Loeys-Dietz syndrome type 1
- Loeys-Dietz syndrome 2 - See Loeys-Dietz syndrome type 2
- Loeys-Dietz syndrome 4 - See Loeys-Dietz syndrome type 4
- Loeys-Dietz syndrome type 1
- Loeys-Dietz syndrome type 2
- Loeys-Dietz syndrome type 3
- Loeys-Dietz syndrome type 4
- Loeys-Dietz syndrome with osteoarthritis - See Loeys-Dietz syndrome type 3
- Loeys-Dietz syndrome, type 1c (formerly) - See Loeys-Dietz syndrome type 3
- Loeys-Dietz syndrome, type 3 - See Loeys-Dietz syndrome type 3
- LOFAD - See Late-Onset Familial Alzheimer Disease
- Logic syndrome - See Epidermolysis bullosa
- Logopenic primary progressive aphasia - See Logopenic progressive aphasia
- Logopenic progressive aphasia
- Logopenic variant PPA - See Logopenic progressive aphasia
- Loiasis
- Loin pain hematuria syndrome
- Loken-Senior syndrome - See Senior Loken Syndrome
- Long bone deficiencies associated with cleft lip-palate - See Roberts syndrome
- Long columella with cleft lip/palate and eye, heart and intestinal anomalies - See Kapur Toriello syndrome
- Long QT syndrome - not a rare disease
- Long QT syndrome 1
- Long QT syndrome 10
- Long QT syndrome 11
- Long QT syndrome 2
- Long QT syndrome 3
- Long QT syndrome 4
- Long QT syndrome 5
- Long QT syndrome 6
- Long QT syndrome 7 - See Andersen-Tawil syndrome
- Long QT syndrome 8 - See Timothy syndrome
- Long QT syndrome 9
- Long QT syndrome with syndactyly - See Timothy syndrome
- Long-chain 3-hydroxy acyl CoA dehydrogenase deficiency - See LCHAD deficiency
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency - See LCHAD deficiency
- Long-chain 3-OH acyl-CoA dehydrogenase deficiency - See LCHAD deficiency
- Long-chain acyl-CoA dehydrogenase deficiency - See LCAD deficiency
- Long-thumb brachydactyly syndrome - See Brachydactyly long thumb type
- Loose anagen hair syndrome
- Loose anagen syndrome - See Loose anagen hair syndrome
- Lopes Gorlin syndrome
- LORD - See Late-onset retinal degeneration
- Loss of all scalp hair - See Alopecia totalis - not a rare disease
- Lota - See Pinta
- Lou Gehrig disease - See Amyotrophic lateral sclerosis
- Louis-Bar syndrome - See Ataxia telangiectasia
- Low tolerance to sound - See Hyperacusis
- Low-birth-weight dwarfism with skeletal dysplasia - See Microcephalic osteodysplastic primordial dwarfism type 1
- Lowe Kohn Cohen syndrome - See Deafness nephritis anorectal malformation
- Lowe oculocerebrorenal syndrome
- Lowe syndrome - See Lowe oculocerebrorenal syndrome
- Lower brachial plexus palsy - See Klumpke paralysis
- Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy with contractures - See Autosomal dominant spinal muscular atrophy, lower extremity-predominant 2
- Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures - SeeAutosomal dominant spinal muscular atrophy, lower extremity-predominant 1
- Lower limb partial duplication renal agenesis - See Billet Bear syndrome
- Lower mesodermal defects - See Lower mesodermal defects sequence
- Lower mesodermal defects sequence
- Low-grade diffuse astrocytoma - See Diffuse astrocytoma
- Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis - See Dent disease
- Lowry Maclean syndrome
- Lowry Wood syndrome
- LP pemphigoides - See Lichen planus pemphigoides
- LP pigmentosa - See Lichen planus pigmentosus
- LP pigmentosus - See Lichen planus pigmentosus
- LPA - See Logopenic progressive aphasia
- LPD - See Disseminated peritoneal leiomyomatosis
- LPHS - See Loin pain hematuria syndrome
- LPI - See Lysinuric protein intolerance
- LPL and HL deficiency - See Lipase deficiency combined
- LPL and HTGL deficiency - See Lipase deficiency combined
- LPL deficiency - See Familial lipoprotein lipase deficiency
- LPP - See Lichen planopilaris
- LPP - See Pustulosis palmaris et plantaris
- LPS - See Van der Woude syndrome
- LQT1 - See Long QT syndrome 1
- LQT10 - See Long QT syndrome 10
- LQT11 - See Long QT syndrome 11
- LQT2 - See Long QT syndrome 2
- LQT3 - See Long QT syndrome 3
- LQT4 - See Long QT syndrome 4
- LQT5 - See Long QT syndrome 5
- LQT6 - See Long QT syndrome 6
- LQT7 - See Andersen-Tawil syndrome
- LQT8 - See Timothy syndrome
- LQT9 - See Long QT syndrome 9
- LRBA deficiency
- LRBA deficiency with Autoantibodies, regulatory T cell defects, Autoimmune Infiltration, and Enteropathy - See LRBA deficiency
- LRCC - See Hereditary leiomyomatosis and renal cell cancer
- LRS - See Larsen syndrome
- LS - See Leigh syndrome
- LSFC - See Leigh syndrome, French Canadian type
- LTBL - See Leukoencephalopathy with thalamus and brainstem involvement and high lactate
- L-tryptophan induced EMS - See Eosinophilia-myalgia syndrome
- Lubag - See X-linked dystonia-parkinsonism/Lubag
- Lubani Al Saleh Teebi syndrome
- Lubinsky syndrome
- Lubs X-linked mental retardation syndrome (formerly) - See MECP2 duplication syndrome
- Lucey-Driscoll syndrome
- Lujan syndrome
- Lumbar malsegmentation short stature
- Lundberg syndrome - See Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome
- Lung adenocarcinoma
- Lung agenesis
- Lung agenesis heart defect thumb anomalies - See Manouvrier syndrome
- Lung nocardiosis - See Nocardiosis
- Lung Small Cell Carcinoma - See Small cell lung cancer
- Lupus - not a rare disease
- Lupus anticoagulant, familial - See Antiphospholipid syndrome
- Lupus erythematosus - See Lupus - not a rare disease
- Lupus erythematosus tumidus
- Lupus erythematosus, cutaneous - See Cutaneous lupus erythematosus
- Lupus nephritis
- Luteinizing hormone releasing hormone, deficiency of with ataxia - See Cerebellar ataxia and hypogonadotropic hypogonadism
- Luteinizing hormone-releasing hormone deficiency with ataxia - See Cerebellar ataxia and hypogonadotropic hypogonadism
- Lutz-Lewandowsky epidermodysplasia verruciformis - See Epidermodysplasia verruciformis
- Lutz-Splendore-Almeida disease - See Paracoccidioidomycosis
- LVM - See Megalencephalic leukoencephalopathy with subcortical cysts
- LVNC - See Left ventricular noncompaction
- LWD - See Leri Weill dyschondrosteosis
- LWNH - See Linear and whorled nevoid hypermelanosis
- LWS - See Lowry Wood syndrome
- L-Xylulose reductase deficiency - See Pentosuria
- L-Xylulosuria - See Pentosuria
- LYH - See Lymphocytic hypophysitis
- Lyme borreliosis - See Lyme disease - not a rare disease
- Lyme disease - not a rare disease
- Lymph Node Neoplasm
- Lymphangiectasia - See Lymphangiectasis
- Lymphangiectasia pulmonary congenital - See Congenital pulmonary lymphangiectasia
- Lymphangiectasies and lymphedema Hennekam type - See Hennekam syndrome
- Lymphangiectasis
- Lymphangioleiomyomatosis
- Lymphangiomas - See Lymphatic malformations
- Lymphangiomatosis
- Lymphangiomatosis pulmonary - See Congenital pulmonary lymphangiectasia
- Lymphangio-myomatosis - See Lymphangioleiomyomatosis
- Lymphangiosarcoma following mastectomy - See Stewart Treves syndrome
- Lymphatic filariasis
- Lymphatic malformations
- Lymphedema and cerebral arteriovenous anomaly
- Lymphedema cholestasis syndrome - See Aagenaes syndrome
- Lymphedema hereditary type 2 - See Hereditary lymphedema type II
- Lymphedema hypoparathyroidism syndrome - See Dahlberg Borer Newcomer syndrome
- Lymphedema praecox - See Hereditary lymphedema type II
- Lymphedema with distichiasis - See Lymphedema-distichiasis syndrome
- Lymphedema with yellow nails - See Yellow nail syndrome
- Lymphedema, microcephaly and chorioretinopathy syndrome
- Lymphedema, atrial septal defect, and characteristic facial changes - See Irons Bhan syndrome
- Lymphedema, hereditary, II - See Hereditary lymphedema type II
- Lymphedema, late-onset - See Hereditary lymphedema type II
- Lymphedema, primary, with myelodysplasia - See Deafness-lymphedema-leukemia syndrome
- Lymphedema-distichiasis syndrome
- Lymphoblastic lymphoma
- Lymphoblastoid variant of NK-cell lymphoma - See Blastic plasmacytoid dendritic cell
- Lymphocyte function-associated antigen 1 immunodeficiency - See Leukocyte adhesion deficiency type 1
- Lymphocytes absent
- Lymphocytic colitis - not a rare disease
- Lymphocytic hypophysitis
- Lymphocytic infiltrate of Jessner
- Lymphocytic mastitis - See Diabetic mastopathy
- Lymphocytic mastopathy - See Diabetic mastopathy
- Lymphocytic vasculitis
- Lymphogranuloma venereum
- Lymphogranulomatosis X - See Angioimmunoblastic T-cell lymphoma
- Lymphoma of the orbit - See Orbital lymphoma
- Lymphoma AIDS related
- Lymphoma, B-Cell - See B-cell lymphoma
- Lymphoma, follicular - See Follicular lymphoma
- Lymphoma, gastric non Hodgkins type
- Lymphoma, Hodgkin's - See Hodgkin lymphoma
- Lymphoma, large-cell
- Lymphoma, large-cell, immunoblastic
- Lymphoma, Lymphoblastic - See Lymphoblastic lymphoma
- Lymphoma, mantle cell - See Mantle cell lymphoma
- Lymphomatoid granulomatosis
- Lymphomatoid papulosis
- Lymphomatous thyroiditis
- Lymphoplasmacytic lymphoma - See Waldenstrom macroglobulinemia
- Lymphoplasmocytic sclerosing pancreatitis - See Autoimmune pancreatitis
- Lymphoproliferative disease, X-linked - See X-linked lymphoproliferative syndrome
- Lymphoproliferative syndrome X-linked 1 - See X-linked lymphoproliferative syndrome 1
- Lymphoproliferative syndrome, X-linked, 1 - See X-linked lymphoproliferative syndrome 1
- Lymphoproliferative syndrome, X-linked, 2 - See X-linked lymphoproliferative syndrome 2
- Lymphosarcoma
- Lynch Lee Murday syndrome - See Caudal appendage deafness
- Lynch syndrome - not a rare disease
- Lynch syndrome 1 - See Lynch syndrome - not a rare disease
- Lynch syndrome 2 - See Lynch syndrome - not a rare disease
- Lyngstadaas syndrome - See Steroid dehydrogenase deficiency dental anomalies
- LyP - See Lymphomatoid papulosis
- Lysine alpha-ketoglutarate reductase deficiency - See Hyperlysinemia
- Lysine intolerance - See Hyperlysinemia
- Lysinuric protein intolerance
- Lysosomal acid lipase deficiency
- Lysosomal alpha-D-mannosidase deficiency - See Alpha-mannosidosis
- Lysosomal beta-mannosidase deficiency - See Mannosidosis, beta A, lysosomal
- Lysosomal cystine transport protein, defect of - See Nephropathic cystinosis
- Lysosomal Free Sialic Acid Storage Disorders - See Free sialic acid storage disease
- Lysosomal glycogen storage disease without acid maltase deficiency (formerly) - See Danon disease
- Lysosomal protective protein deficiency of - See Galactosialidosis
- Lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues - SeeFucosidosis
- Lyssa - See Rabies
domingo, 27 de enero de 2019
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program
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