Disease Index

9,486 diseases
early-onset posterior subcapsular cataract
human disease
early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome
human disease
early-onset schizophrenia
human disease
early-onset X-linked optic atrophy
MeSH: C537125
EAST syndrome
SeSAME syndrome is characterized by seizures, sensorineural deafness, ataxia, intellectual deficit, and electrolyte imbalance (hypokalemia, metabolic alkalosis, and hypomagnesemia)
MeSH: C557674
East Texas bleeding disorder
human disease
MeSH: C565275
Eastern equine encephalitis
horse disease
MeSH: D020242
eating seizures
human disease
Ebola hemorrhagic fever
human disease
ICD: A98.4MeSH: D019142
Ebstein anomaly
tricuspid valve disease that is a congenital heart defect in which the septal leaflet of the tricuspid valve is displaced towards the apex of the right ventricle of the heart
MeSH: D004437
ectasia of the left appendage
human disease
ectasia of the right atrial appendage
human disease
ectodermal dysplasia
human disease
ICD: Q82.4MeSH: D004476
ectodermal dysplasia Margarita type
human disease
ectodermal dysplasia with adrenal cyst
human disease
MeSH: C538015
Ectodermal dysplasia with corkscrew hairs
human disease
MeSH: C536565
ectodermal dysplasia with natal teeth, Turnpenny type
human disease
MeSH: C563347
ectodermal dysplasia-cutaneous syndactyly syndrome
human disease
ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome
MeSH: C565605
ectodermal dysplasia-sensorineural deafness syndrome
human disease
MeSH: C535757
ectodermal dysplasia-syndactyly syndrome
human disease
ectodermal dysplasia-syndactyly syndrome 1
human disease
ectodermal dysplasia, trichoodontoonychial type
MeSH: C565068
ectodermal malformation syndrome associated with ocular features
human disease
ectopia cordis
congenital malformation in which the heart is abnormally located either partially or totally outside of the thorax
ICD: Q24.8MeSH: D054083
ectopia lentis
disorder of lens
ICD: H27.1MeSH: D004479
ectopia lentis-chorioretinal dystrophy-myopia syndrome
MeSH: C536124
ectopic aldosterone-producing tumor
human disease
ectopic Cushing syndrome
human disease
MeSH: D000182
ectrodactyly
deficiency or absence of one or more central digits of the hand or foot
ICD: Q71.671.6MeSH: C574275
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