|
641
|
|
|
Lysyl oxidase like 3 |
LOXL, MYP28 |
|
|
642
|
|
|
Ligand of numb-protein X 1 |
LNX, MPDZ, PDZRN2 |
|
|
643
|
|
|
Lamin B2 |
EPM9, LAMB2, LMN2, MCPH27 |
Acquired partial lipodystrophy, Action myoclonus-renal failure syndrome, Amyotrophy, Colorectal cancer, Dentatorubral pallidoluysian atrophy, Developmental delay, Diabetes mellitus, Fatty liver, Glomerulonephritis, Hypoplasia of thumb, Immunologic deficiency syndromes, Inclusion-body disease, Lipoatrophy, Lipodystrophy, Lymphocytosis, May-white syndrome, Mental retardation, Microglossia, Myoclonic epilepsy, Myopathy, Nephrotic syndrome, Polycystic ovary syndrome, Progressive myoclonic epilepsy, Renal glomerular disease, Scoliosis, Status epilepticusView all (11 more) |
|
644
|
|
|
Leucine rich repeat and Ig domain containing 1 |
LERN1, LRRN6A, MRT64, UNQ201 |
|
|
645
|
|
|
Leucine rich repeat and coiled-coil centrosomal protein 1 |
CLERC, CLERK, SAP2, VFL1 |
|
|
646
|
|
|
Leucine rich repeat containing G protein-coupled receptor 5 |
FEX, GPR49, GPR67, GRP49, HG38 |
|
|
647
|
|
|
Lymphocyte antigen 6 family member D |
E48, Ly-6D |
|
|
648
|
|
|
Lin-7 cell polarity scaffold A |
LIN-7A, LIN7, MALS-1, MALS1, TIP-33, VELI1 |
|
|
649
|
|
|
LIM domain binding 1 |
CLIM-2, CLIM2, LDB-1, NLI |
|
|
650
|
|
|
LIM homeobox 4 |
CPHD4 |
Agenesis of corpus callosum, Central hypothyroidism, Congenital exomphalos, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes insipidus, Dwarfism, Dyssomnia, Ectopic anterior pituitary gland, Holoprosencephaly, Hypoglycemia, Hypogonadotropic hypogonadism, Hypopituitarism, Hypothyroidism, Leukemia, Mental retardation, Oral cleft, Osteopenia, Osteoporosis of vertebrae, Physiologic amenorrhea, Pituitary dwarfism, Pituitary hormone deficiency, Pituitary stalk interruption syndrome, Polydactyly, Septo-optic dysplasia, Short stature-pituitary and cerebellar defects-small sella turcica syndrome, Sleep disordersView all (13 more) |
