|
mental retardation, autosomal dominant 49; MRD49
|
http://purl.obolibrary.org/obo/MONDO_0030914 |
|
|
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
|
914 |
|
|
cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1; CADASIL1
|
http://purl.obolibrary.org/obo/MONDO_0000914 |
|
|
GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 18; GPIBD18
|
http://purl.obolibrary.org/obo/MONDO_0029140 |
|
|
Dias-Logan syndrome; DILOS
|
14914 |
|
|
INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF
|
http://purl.obolibrary.org/obo/MONDO_0029143 |
|
|
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY
|
29144 |
|
|
EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY; EHMTO
|
http://purl.obolibrary.org/obo/MONDO_0029144 |
|
|
primary dystonia, DYT2 type
|
9141 |
|
|
METHANETHIOL Oxidase Deficiency
|
29144 |
|
|
SCHOPF-Schulz-Passarge syndrome; SSPS
|
http://purl.obolibrary.org/obo/MONDO_0009145 |
|
|
SAUL-WILSON SYNDROME; SWILS
|
http://purl.obolibrary.org/obo/MONDO_0029146 |
|
|
dyssegmental dwarfism Silverman-Handmaker type
|
9140 |
|
