Disease Index
9,486 diseaseslipid storage disease
lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues
MeSH: D008064
lipoatrophia semicircularis
medical condition
ICD: L90.8
lipoatrophic diabetes
type 2 diabetes that involves severe lipodystrophy in addition to the traditional signs of diabetes
MeSH: D003923
lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy
human disease
lipoblastoma
medical condition
MeSH: D062689
lipodystrophy due to peptidic growth factors deficiency
lipodystrophy-intellectual disability-deafness syndrome
MeSH: C564283
lipoic acid biosynthesis defect
human disease
lipoic acid synthetase deficiency
disease
lipoid congenital adrenal hyperplasia
medical condition
MeSH: C537027
lipoid proteinosis
rare recessive genetic disorder
ICD: E78.8MeSH: D008065
lipoma associated with neurospinal dysraphism
human disease
lipomyelomeningocele
Birth defect
MeSH: C537030
lipoprotein glomerulopathy
human disease
MeSH: C567089
liposarcoma
lipomatous cancer that arises in fat cells in deep soft tissue retroperitoneum
MeSH: D008080
Lipoyl transferase 1 deficiency
human disease
Lipoyl transferase 2 deficiency
human disease
Lisch epithelial corneal dystrophy
Human disease
MeSH: C567588
lissencephaly
brain disorder that prevents growth of brain folds
MeSH: D054082
lissencephaly due to LIS1 mutation
human disease
lissencephaly due to TUBA1A mutation
lissencephaly type 1 due to doublecortin gene mutation
human disease
lissencephaly type 3
human disease
lissencephaly type 3-familial fetal akinesia sequence syndrome
lissencephaly type 3-metacarpal bone dysplasia syndrome
MeSH: C563383
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 C (LCHc) is a severe form of lissencephaly with cerebellar hypoplasia characterized by severe microcephaly, cleft palate, and severe cerebellar and brainstem hypoplasia leading to neonatal death
lissencephaly with cerebellar hypoplasia type D