Preferred Name | hereditary neurological disease | |
Synonyms |
neurogenetic disease |
|
Definitions |
A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0100545 |
|
creator | ||
definition |
A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles. |
|
has_exact_synonym |
neurogenetic disease |
|
IAO_0000233 | ||
id |
MONDO:0100545 |
|
label |
hereditary neurological disease |
|
notation |
MONDO:0100545 |
|
prefLabel |
hereditary neurological disease |
|
treeView | ||
subClassOf |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.obolibrary.org/obo/MONDO_0100545 | GCBO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0100545 | CCONT | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0100545 | EFO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0100545 | EFO | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0100545 | OBA | SAME_URI | |
http://purl.obolibrary.org/obo/MONDO_0100545 | GCBO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100545 | CCONT | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100545 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100545 | EFO | LOOM | |
http://purl.obolibrary.org/obo/MONDO_0100545 | OBA | LOOM |