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Rare conditions starting with L
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227 conditions starting with L
- L-2-hydroxyglutaric aciduria
- L-ferritin deficiency
- L1 syndrome
- La Crosse encephalitis
- Lafora disease
- LAMA2-related muscular dystrophy
- LAMA5-related multisystemic syndrome
- Lamb-Shaffer syndrome
- Lambert syndrome
- Lamellar ichthyosis
- Landau-Kleffner syndrome
- Langer mesomelic dysplasia syndrome
- Langer-Giedion syndrome
- Langerhans cell histiocytosis
- Langerhans cell sarcoma
- Large congenital melanocytic nevus
- Large-cell immunoblastic lymphoma
- Laron-type isolated somatotropin defect
- Larsen syndrome
- Larsen-like osseous dysplasia-short stature syndrome
- Larsen-like syndrome, B3GAT3 type
- Laryngeal abductor paralysis with intellectual disability syndrome
- Laryngeal atresia
- Laryngeal papillomatosis
- Laryngo-onycho-cutaneous syndrome
- Laryngocele
- Laryngotracheoesophageal cleft
- Lassa fever
- Late-infantile neuronal ceroid lipofuscinosis
- Late-onset junctional epidermolysis bullosa
- Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
- Late-onset retinal degeneration
- Lateral meningocele syndrome
- Laterality defects, autosomal dominant
- Lathosterolosis
- Lattice corneal dystrophy Type I
- Laurence-Moon syndrome
- Laurin-Sandrow syndrome
- LCAT deficiency
- Lead poisoning
- Leber congenital amaurosis
- Leber congenital amaurosis 2
- Leber optic atrophy
- Leber plus disease
- Left ventricular noncompaction
- Legg-Calve-Perthes disease
- Legionnaires' disease
- Legius syndrome
- Leigh syndrome
- Leiomyoma of vulva and esophagus
- Leiomyosarcoma
- Leishmaniasis
- Lelis syndrome
- Lennox-Gastaut syndrome
- Lens coloboma
- Lenz microphthalmia syndrome
- Lenz-Majewski hyperostosis syndrome
- Leprosy
- Leptomyelolipoma
- Leptospirosis
- Leri pleonosteosis
- Leri-Weill dyschondrosteosis
- Lesch-Nyhan syndrome
- Lethal acantholytic epidermolysis bullosa
- Lethal arteriopathy syndrome due to fibulin-4 deficiency
- Lethal arthrogryposis-anterior horn cell disease syndrome
- Lethal chondrodysplasia, Seller type
- Lethal congenital contracture syndrome
- Lethal congenital contracture syndrome 1
- Lethal congenital contracture syndrome 11
- Lethal congenital contracture syndrome 2
- Lethal congenital contracture syndrome 3
- Lethal congenital contracture syndrome 4
- Lethal congenital glycogen storage disease of heart
- Lethal faciocardiomelic dysplasia
- Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
- Lethal hemolytic anemia-genital anomalies syndrome
- Lethal hydranencephaly-diaphragmatic hernia syndrome
- Lethal infantile mitochondrial myopathy
- Lethal Kniest-like dysplasia
- Lethal Kniest-like syndrome
- Lethal Larsen-like syndrome
- Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome
- Lethal multiple pterygium syndrome
- Lethal occipital encephalocele-skeletal dysplasia syndrome
- Lethal omphalocele-cleft palate syndrome
- Lethal osteosclerotic bone dysplasia
- Lethal polymalformative syndrome, Boissel type
- Lethal recessive chondrodysplasia
- Lethal short-limb skeletal dysplasia, Al Gazali type
- Lethal tight skin contracture syndrome
- Leukocyte adhesion deficiency
- Leukocyte adhesion deficiency 1
- Leukocyte adhesion deficiency type II
- Leukodystrophy
- Leukoencephalopathy with bilateral anterior temporal lobe cysts
- Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome
- Leukoencephalopathy with calcifications and cysts
- Leukoencephalopathy with mild cerebellar ataxia and white matter edema
- Leukoencephalopathy-palmoplantar keratoderma syndrome
- Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome
- Leukoencephalopathy, diffuse hereditary, with spheroids 1
- Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
- Leukonychia totalis
- Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome
- Levy-Hollister syndrome
- Lewis-Sumner syndrome
- Leydig cell hypoplasia
- Lhermitte-Duclos disease
- Li-Fraumeni syndrome
- Lichen planopilaris
- Lichen planus pemphigoides
- Lichen planus pigmentosus
- Lichtenstein syndrome
- Lichtenstein-Knorr syndrome
- Liddle syndrome
- Light chain deposition disease
- Ligneous conjunctivitis
- Limb body wall complex
- Limb-girdle muscular dystrophy
- Limb-girdle muscular dystrophy due to POMK deficiency
- Limb-mammary syndrome
- Limbic encephalitis
- Limbic encephalitis with LGI1 antibodies
- Limited cutaneous systemic sclerosis
- Linear and whorled nevoid hypermelanosis
- Linear atrophoderma of Moulin
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
- Linear lichen planus
- Linear nevus sebaceous syndrome
- Linear porokeratosis
- Linear scleroderma
- Linear skin defects with multiple congenital anomalies
- Linear verrucous nevus syndrome
- Lip and oral cavity carcinoma
- Lipase deficiency, combined
- LIPE-related familial partial lipodystrophy
- Lipid proteinosis
- Lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy
- Lipoblastoma
- Lipodermatosclerosis
- Lipodystrophy due to peptidic growth factors deficiency
- Lipodystrophy-intellectual disability-deafness syndrome
- Lipoic acid synthetase deficiency
- Lipoid nephrosis
- Lipomatosis dolorosa
- Lipomyelomeningocele
- Lipoprotein glomerulopathy
- Liposarcoma
- Lipoyl transferase 1 deficiency
- Lisch epithelial corneal dystrophy
- Lissencephaly
- Lissencephaly due to LIS1 mutation
- Lissencephaly due to TUBA1A mutation
- Lissencephaly type 1 due to doublecortin gene mutation
- Lissencephaly type 3-familial fetal akinesia sequence syndrome
- Lissencephaly type 3-metacarpal bone dysplasia syndrome
- Lissencephaly with cerebellar hypoplasia
- Lissencephaly with cerebellar hypoplasia type A
- Lissencephaly with cerebellar hypoplasia type B
- Lissencephaly with cerebellar hypoplasia type C
- Lissencephaly with cerebellar hypoplasia type D
- Lissencephaly with cerebellar hypoplasia type E
- Lissencephaly with cerebellar hypoplasia type F
- Listeriosis
- Littoral cell angioma
- Livedoid vasculopathy
- Liver angiosarcoma
- Liver mesenchymal hamartoma
- LMNA-related cardiocutaneous progeria syndrome
- Localized Castleman disease
- Localized dystrophic epidermolysis bullosa
- Localized junctional epidermolysis bullosa, non-Herlitz type
- Localized lichen myxedematosus
- Localized lipodystrophy
- Localized scleroderma
- Locked-in syndrome
- Loeys-Dietz syndrome
- Loeys-Dietz syndrome 1
- Loeys-Dietz syndrome 2
- Loeys-Dietz syndrome 4
- Logopenic progressive aphasia
- Loiasis
- Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
- Long chain acyl-CoA dehydrogenase deficiency
- Long QT syndrome
- Long QT syndrome 10
- Long QT syndrome 11
- Long QT syndrome 2
- Long QT syndrome 3
- Long QT syndrome 5
- Long QT syndrome 6
- Long QT syndrome 9
- Loose anagen hair syndrome
- Loricrin keratoderma
- Low phospholipid associated cholelithiasis
- Lowe syndrome
- Lowe-Kohn-Cohen syndrome
- Lower eyelid coloboma
- Lower limb deficiency-hypospadias syndrome
- Lower motor neuron syndrome with late-adult onset
- Lown-Ganong-Levine syndrome
- Lowry-MacLean syndrome
- Lowry-Wood syndrome
- LRP5-related primary osteoporosis
- Lucey-Driscoll syndrome
- Lujo hemorrhagic fever
- Lung agenesis-heart defect-thumb anomalies syndrome
- Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome
- Lung lymphangioleiomyomatosis
- Lupus erythematosus tumidus
- Lupus nephritis
- Lymph node neoplasm
- Lymphangiomyomatosis
- Lymphatic malformation 6
- Lymphedema praecox
- Lymphedema-atrial septal defects-facial changes syndrome
- Lymphedema-cerebral arteriovenous anomaly syndrome
- Lymphedema-posterior choanal atresia syndrome
- Lymphoblastic lymphoma
- Lymphoma, Hodgkin, X-linked pseudoautosomal
- Lymphomatoid granulomatosis
- Lymphomatoid papulosis
- Lymphoproliferative syndrome 1
- Lymphosarcoma
- Lysinuric protein intolerance
- Lysosomal acid lipase deficiency
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