Search Diseases
???pagination.result.count???
???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 10 11 12 13 ???pagination.result.next???
Disease | Synonyms | Description | Articles | Phenotypes |
---|---|---|---|---|
leukoencephalopathy with vanishing white matter 2 |
|
A leukoencephalopathy with vanishing white matter ..[+]
|
||
lymphoblastic lymphoma |
|
A lymphoma that has_material_basis_in immature mal..[+]
|
||
lupus nephritis |
|
A glomerulonephritis that is characterized by infl..[+]
|
||
lung mucinous cystadenocarcinoma |
|
A lung adenocarcinoma that is a very rare malignan..[+]
|
||
laryngomalacia |
congenital laryngomalacia
|
A laryngeal disease that is characterized by inwar..[+]
|
||
long COVID |
chronic COVID-19; PASC; post-acute sequelae of SAR..
[+]
|
A Coronavirus infectious disease that is character..[+]
|
||
Leber congenital amaurosis 19 |
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
lacrimoauriculodentodigital syndrome 3 |
Lacrimo-auriculo-dento-digital syndrome 3
|
A LADD syndrome that is characterized by aplasia, ..[+]
|
||
lethal congenital glycogen storage disease of heart |
fatal congenital nonlysosomal cardiac glycogenosis..
[+]
|
A glycogen storage disease characterized by autoso..[+]
|
||
Leber congenital amaurosis 9 |
LCA9
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 2 |
LCA2; amaurosis congenita of Leber II
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 1 |
LCA1; amaurosis congenita of Leber I
|
A Leber congenital amaurosis characterized by seve..[+]
|
||
Leber congenital amaurosis 8 |
LCA8
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 12 |
LCA12
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 16 |
LCA16
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 14 |
LCA14
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 15 |
LCA15
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 5 |
LCA5
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 11 |
LCA11
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 17 |
LCA17
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 10 |
LCA10
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 6 |
LCA6
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 13 |
LCA13
|
A Leber congenital amaurosis thatis characterized ..[+]
|
||
Leber congenital amaurosis 3 |
LCA3
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
Leber congenital amaurosis 4 |
LCA4
|
A Leber congenital amaurosis that is characterized..[+]
|
||
Leber congenital amaurosis 7 |
LCA7
|
A Leber congenital amaurosis that has_material_bas..[+]
|
||
late-adult onset retinitis pigmentosa |
senile retinitis pigmentosa
|
A retinitis pigmentosa that is characterized by on..[+]
|
||
long QT syndrome 1 |
LQT1; ventricular fibrillation with prolonged QT i..
[+]
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 2 |
LQT2
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 3 |
LQT3
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 5 |
LQT5
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 6 |
LQT6
|
A long QT interval syndrome that has_material_basi..[+]
|
||
long QT syndrome 9 |
LQT9
|
A long QT syndrome that has_material_basis_in muta..[+]
|
||
long QT syndrome 10 |
LQT10
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 11 |
LQT11
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 12 |
LQT12
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 13 |
LQT13
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 14 |
LQT14
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
long QT syndrome 15 |
LQT15
|
A long QT syndrome that has_material_basis_in domi..[+]
|
||
leukocyte adhesion deficiency 1 |
lymphocyte function-associated antigen 1 immunodef..
[+]
|
A leukocyte adhesion deficiency that has_material_..[+]
|
||
leukocyte adhesion deficiency 3 |
A leukocyte adhesion deficiency that is characteri..[+]
|
|||
large congenital melanocytic nevus |
LCMN; Congenital pigmented nevus; Giant congenital..
[+]
|
A skin disease characterized by the presence at bi..[+]
|
||
Li-Fraumeni syndrome 1 |
LFS1
|
A Li-Fraumeni syndrome that has_material_basis_in ..[+]
|
||
linear nevus sebaceous syndrome |
Jadassohn nevus phakomatosis; JNP; nevus sebaceus ..
[+]
|
A syndrome characterized by sebaceous nevi typical..[+]
|
||
long QT syndrome 4 |
LQT4
|
A long QT syndrome that has_material_basis_in hete..[+]
|
||
low molecular weight proteinuria with hypercalciuric nephrocalcinosis |
|
A Dent disease characterized by elevted levels of ..[+]
|
||
lissencephaly 10 |
LIS10
|
A lissencephaly characterized by variably delayed ..[+]
|
||
lissencephaly 4 |
lissencephaly 4 with microcephaly; LIS4
|
A microlissencephaly characterized by lissencephal..[+]
|
||
lissencephaly 1 |
LIS1; PAFAH1B1-related lissencephaly
|
A lissencephaly characterized by an abnormally thi..[+]
|
||
Leydig cell hypoplasia |
46,XY disorder of sex development due to LH resist..
[+]
|
A pseudohermaphroditism that has_material_basis_in..[+]
|
???pagination.result.page??? ???pagination.result.prev??? 1 2 3 4 5 6 7 8 9 10 11 12 13 ???pagination.result.next???