Search Diseases
???pagination.result.count???
???pagination.result.page??? ???pagination.result.prev??? 4 5 6 7 8 9 10 11 12 13 14 15 16 ???pagination.result.next???
Disease | Synonyms | Description | Articles | Phenotypes |
---|---|---|---|---|
low tension glaucoma |
Normal tension glaucoma
|
An open-angle glaucoma characterized by increased ..[+]
|
||
angle-closure glaucoma |
Narrow cleft glaucoma; ACG - Angle-closure glaucom..
[+]
|
A glaucoma characterized by closure of the anterio..[+]
|
||
kwashiorkor |
Nutritional oedema with dyspigmentation of skin an..
[+]
|
A protein-energy malnutrition that is characterize..[+]
|
||
vestibular nystagmus |
Nystagmus associated with disorder of the vestibul..
[+]
|
n_a
|
1 articles | |
abducens nerve neoplasm |
n_a
|
|||
central neurocytoma |
Neurolipocytoma
|
n_a
|
||
disease of cellular proliferation |
neoplasm; cell process disease
|
A disease that is characterized by abnormally rapi..[+]
|
148 articles | 98 matches |
La Crosse encephalitis |
Neuroinvasive California encephalitis virus infect..
[+]
|
A viral infectious disease that results_in inflamm..[+]
|
||
polycystic echinococcosis |
neotropical echinococcosis; human polycystic hydat..
[+]
|
An echinococcosis that is caused by the larvae of ..[+]
|
||
primary amebic meningoencephalitis |
Naegleria fowleri infection
|
A parasitic protozoa infectious disease that invol..[+]
|
||
Farber lipogranulomatosis |
A lipid storage disease that is characterized by a..[+]
|
|||
Carney complex |
NAME Syndrome; Carney Complex, Type 2; Carney Synd..
[+]
|
A syndrome characterized by myxomas, spotty pigmen..[+]
|
||
proteasome-associated autoinflammatory syndrome 1 |
A proteasome-associated autoinflammatory syndrome ..[+]
|
|||
hereditary lymphedema |
Nonne-Milroy lymphedema; Milroy's disease
|
A lymphedema commonly located_in legs, caused_by c..[+]
|
1 articles | |
biliary tract benign neoplasm |
A hepatobiliary benign neoplasm located_in the bil..[+]
|
|||
Athabaskan brainstem dysgenesis syndrome |
NAVAJO BRAINSTEM SYNDROME
|
A brain disease that is characterized by brainstem..[+]
|
||
cerebral folate receptor alpha deficiency |
Neurodegeneration due to cerebral folate transport..
[+]
|
A vitamin metabolic disorder that has_material_bas..[+]
|
||
Chanarin-Dorfman syndrome |
neutral lipid storage disease; Chanarin-Dorfman sy..
[+]
|
A lipid storage disease that is characterized by a..[+]
|
||
mature T-cell and NK-cell lymphoma |
NK-T cell lymphoma; mature T-cell and natural kill..
[+]
|
A T-cell non-Hodgkin lymphoma that has_material_ba..[+]
|
||
Ogden syndrome |
A syndrome characterized by postnatal growth failu..[+]
|
|||
Muckle-Wells syndrome |
neutrophilic urticaria; MWS
|
A syndrome characterized by episodic skin rash, ar..[+]
|
||
connective tissue benign neoplasm |
A musculoskeletal system benign neoplasm that is l..[+]
|
|||
dentatorubral-pallidoluysian atrophy |
Naito-Oyanagi disease; DRPLA; Haw River Syndrome
|
An autosomal dominant cerebellar ataxia that has_m..[+]
|
||
mitochondrial complex V (ATP synthase) deficiency nuclear type 2 |
neonatal mitochondrial encephalocardiomyopathy due..
[+]
|
A mitochondrial complex V (ATP synthase) deficienc..[+]
|
||
Galloway-Mowat syndrome 1 |
A Galloway-Mowat syndrome that has_material_basis_..[+]
|
2 articles | 21 matches | |
chromosome 17q11.2 deletion syndrome |
A chromosomal deletion syndrome that has_material_..[+]
|
|||
Kabuki syndrome |
Niikawa-Kuroki syndrome; Kabuki make up syndrome; ..
[+]
|
A syndrome characterized by multiple congenital an..[+]
|
4 articles | 27 matches |
Perlman syndrome |
nephroblastomatosis, fetal ascites, macrosomia and..
[+]
|
A syndrome characterized by polyhydramnios with ne..[+]
|
||
chondrodysplasia-pseudohermaphroditism syndrome |
Nivelon-Nivelon-Mabille syndrome; chondrodysplasia..
[+]
|
A syndrome characterized by the clinical features ..[+]
|
||
autosomal recessive congenital ichthyosis |
non bullous congenital ichthyosiform erythroderma; ..
[+]
|
An ichthyosis that is characterized by autosomal r..[+]
|
||
autosomal dominant nocturnal frontal lobe epilepsy 1 |
nocturnal frontal lobe epilepsy 1; ENFL1
|
An autosomal dominant nocturnal frontal lobe epile..[+]
|
1 articles | |
autosomal dominant nocturnal frontal lobe epilepsy 2 |
nocturnal frontal lobe epilepsy 2; ENFL2
|
An autosomal dominant nocturnal frontal lobe epile..[+]
|
2 articles | |
autosomal dominant nocturnal frontal lobe epilepsy 3 |
nocturnal frontal lobe epilepsy 3; ENFL3
|
An autosomal dominant nocturnal frontal lobe epile..[+]
|
||
autosomal dominant nocturnal frontal lobe epilepsy 4 |
nocturnal frontal lobe epilepsy 4; ENFL4
|
An autosomal dominant nocturnal frontal lobe epile..[+]
|
||
autosomal dominant nocturnal frontal lobe epilepsy 5 |
nocturnal frontal lobe epilepsy 5; ENFL5
|
An autosomal dominant nocturnal frontal lobe epile..[+]
|
1 articles | |
autosomal dominant auditory neuropathy 1 |
An autosomal dominant nonsyndromic deafness charac..[+]
|
|||
autosomal recessive congenital ichthyosis 2 |
An autosomal recessive congenital ichthyosis chara..[+]
|
|||
isolated growth hormone deficiency |
non-acquired isolated growth hormone deficiency; c..
[+]
|
A hypopituitarism characterized by abnormally low ..[+]
|
||
Y-linked spermatogenic failure 2 |
nonobstructive Y-linked spermatogenic failure; SPG..
[+]
|
A spermatogenic failure that is characterized by n..[+]
|
||
hereditary lymphedema I |
Nonne-Milroy lymphedema; congenital primary lymphe..
[+]
|
A hereditary lymphedema characterized by autosomal..[+]
|
||
progressive familial intrahepatic cholestasis 5 |
NR1H4 deficiency; PFIC5
|
A progressive familial intrahepatic cholestasis ch..[+]
|
||
primary coenzyme Q10 deficiency 7 |
neonatal encephalomyopathy-cardiomyopathy-respirat..
[+]
|
A primary coenzyme Q10 deficiency that has_materia..[+]
|
||
primary autosomal recessive microcephaly 15 |
neurodevelopmental disorder with progressive micro..
[+]
|
A primary autosomal recessive microcephaly charact..[+]
|
||
schwannomatosis 1 |
neurofibromatosis 3; SMARCB1-related schwannomatos..
[+]
|
A schwannomatosis that has_material_basis_in germl..[+]
|
||
schwannomatosis 2 |
neurofibromatosis 3; LZTR1-related schwannomatosis..
[+]
|
A schwannomatosis that has_material_basis_in germl..[+]
|
||
Legius syndrome |
A RASopathy characterized by multiple cafe-au-lait..[+]
|
|||
Halperin-Birk syndrome |
NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLE..
[+]
|
A syndrome characterized by structural brain defec..[+]
|
||
otospondylomegaepiphyseal dysplasia, autosomal recessive |
An osteochondrodysplasia that results from mutatio..[+]
|
|||
intestinal pseudo-obstruction |
neuronal intestinal dysplasia; Chronic intestinal ..
[+]
|
A colonic disease that is characterized by bowel o..[+]
|
||
mitochondrial DNA depletion syndrome 6 |
Navajo neurohepatopathy; MPV17-related hepatocereb..
[+]
|
A mitochondrial DNA depletion syndrome that is cha..[+]
|
???pagination.result.page??? ???pagination.result.prev??? 4 5 6 7 8 9 10 11 12 13 14 15 16 ???pagination.result.next???