back 1
2
3
5
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
R
S
T
U
V
W
X
Y
Z
List of all diseases starting with L
- L-ARABINOSURIA MIM=---
- LACTASE DEFICIENCY, CONGENITAL MIM=223000
- LACTATE DEHYDROGENASE B DEFICIENCY (LDHBD) MIM=614128
- LACTOSE INTOLERANCE MIM=150220
- LACTOSE INTOLERANCE, ADULT TYPE MIM=223100
- LANOSTEROL DEMETHYLASE DEFICIENCY MIM=601637
- LATHOSTEROLOSIS MIM=607330
- LEBER CONGENITAL AMAUROSIS 11; LCA11 MIM=613837
- LEBER OPTIC ATROPHY AND DYSTONIA (LDYT) MIM=500001
- LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) MIM=535000
- LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY MIM=245900
- LEIGH SYNDROME, FRENCH CANADIAN TYPE (LSFC) MIM=220111
- LEIGH`S SYNDROME, SUBACUTE NECROTIZING ENCEPHALOPATHY (SNE) MIM=256000
- LEPTIN DEFICIENCY OR DYSFUNCTION; LEPD MIM=614962
- LEPTIN RECEPTOR DEFICIENCY MIM=614963
- LESCH-NYHAN SYNDROME (HGPRT, HPRT) MIM=300322
- LETHAL INFANTILE MITOCHONDRIAL DISEASE (LIMM) MIM=551000
- LEUKODYSTROPHY, PROGRESSIVE, EARLY CHILDHOOD-ONSET; PLDECO MIM=617762
- LEUKOENCEPHALOPATHY WITH BRAINSTEM AND SPINAL CORD INVOLVEMENT AND LACTATE ELEVATION (LBSL) MIM=611105
- LEUKOTRIENE C4-SYNTHESIS DEFICIENCY MIM=614037
- LIPID STORAGE MYOPATHY DUE TO FLAVIN ADENINE DINUCLEOTIDE SYNTHETASE DEFICIENCY; LSMFLAD MIM=255100
- LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1; CGL1 MIM=608594
- LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2; CGL2 MIM=269700
- LIPOID ADRENAL HYPERPLASIA (StAR DEFICIENCY) MIM=201710
- LIPOYLTRANSFERASE 1 DEFICIENCY (LIPT1D) MIM=616299
- LIPOYLTRANSFERASE 2 DEFICIENCY (LIPT2D); NELABA MIM=617668
- LIVER DISEASE, LIVER FAILURE, UNSPECIFIC [DD] MIM=
- LIVER FAILURE, INFANTILE, TRANSIENT (LFIT) MIM=613070
- LONG CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (LCAD) MIM=201475
- LONG-CHAIN FATTY ACIDS, DEFECT IN TRANSPORT OF MIM=603376
- LONG-CHAIN-3-HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (LCHAD) MIM=609016
- LYSINURIC PROTEIN INTOLERANCE (LPI) MIM=222700
- LYSOSOMAL ACID LIPASE DEFICIENCY; LAL-D MIM=278000