achalasia (disease)

MONDO_0008698 Condition
achalasia of esophagus

mesoaxial synostotic syndactyly with phalangeal reduction

MONDO_0012271 Condition
Syndactyly type 9

holoprosencephaly 8

MONDO_0012267 Condition
holoprosencephaly type 8

epileptic encephalopathy, early infantile, 3

MONDO_0012245 Condition
Epileptic Encephalopathy, Early Infantile, type 3

progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2

MONDO_0012238 Condition
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant type 2

hepatoencephalopathy due to combined oxidative phosphorylation defect type 1

MONDO_0012191 Condition
Hepatoencephalopathy due to COXPD1

microphthalmia, isolated, with coloboma 10

MONDO_0014635 Condition
Microphthalmia, Isolated, With Coloboma type 10

cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3

MONDO_0014667 Condition
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency type 3

bone dysplasia, lethal Holmgren type

MONDO_0008878 Condition
Autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type

hydrolethalus syndrome

MONDO_0006037 Condition
Salonen-Herva-Norio syndrome

obsolete western equine encephalitis

MONDO_0006017 Condition

obsolete West Nile encephalitis

MONDO_0006016 Condition

viral encephalitis

MONDO_0006009 Condition
Viral Encephalitis

Venezuelan equine encephalitis

MONDO_0006005 Condition