Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "L"

621 to 630 of 673 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
621	8022	LHX3	LIM homeobox 3	CPHD3, LIM3, M2-LHX3	Adrenocorticotropic hormone deficiency, Atrial fibrillation, Central hypothyroidism, Congenital exomphalos, Developmental delay, Dwarfism, Dyssomnia, Gonadotropin deficiency, Hearing loss, Hypogonadism, Hypothyroidism, Isolated somatotropin deficiency, Mental retardation, Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome, Oral cleft View all (6 more)
622	80350	LPAL2	Lipoprotein(a) like 2 (pseudogene)	APOA2, APOAL, APOARGC, apo(a)rg-C	Coronary artery disease, Coronary heart disease
623	80740	LY6G6C	Lymphocyte antigen 6 family member G6C	C6orf24, G6c, NG24	Diabetes mellitus, Hodgkin disease, Lupus erythematosus, Rheumatoid arthritis
624	80741	LY6G5C	Lymphocyte antigen 6 family member G5C	C6orf20, G5C, LY6G5CA, LY6G5CB, NG33	Diabetes mellitus, Rheumatoid arthritis
625	80774	LIMD2	LIM domain containing 2	-	Breast cancer, Mammary neoplasms, Breast carcinoma, Marfan syndrome
626	80856	LNPK	Lunapark, ER junction formation factor	KIAA1715, LNP, LNP1, NEDEHCC, Ul, ulnaless	Cerebellar atrophy, Developmental delay, Hypoplasia of corpus callosum, Mental retardation, Myoclonic seizures, Neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum
627	81543	LRRC3	Leucine rich repeat containing 3	C21orf102, C21orf30, LRRC3DN	Intracranial aneurysm
628	81562	LMAN2L	Lectin, mannose binding 2 like	MRD69, MRT52, VIPL	Absence of septum pellucidum, Autism, Bipolar disorder, Central visual impairment, Cerebral atrophy, Chromophobe carcinoma, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Epilepsy, Hypoplasia of corpus callosum, Mental retardation, Manic disorder, Mental depression View all (11 more)
629	81606	LBH	LBH regulator of Wnt signaling pathway	-	Lupus erythematosus, Vulval varices
630	81887	LAS1L	LAS1 like ribosome biogenesis factor	Las1, Las1-like, MRXSWTS, WTS, dJ475B7.2	Brachycephaly, Colorectal cancer, Cryptorchidism, Developmental delay, Dwarfism, Gynecomastia, Hypogonadism, Hypogonadotropic hypogonadism, Mental retardation, Mental retardation, x-linked, Microcephaly, Micrognathism, Microtia, Mood swings, Obesity View all (4 more)

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