12 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
| DOID:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| DOID:0080015 | physical disorder | A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment. |
| DOID:0050737 | autosomal recessive disease | An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. |
| DOID:2490 | congenital nervous system abnormality | |
| DOID:0050453 | lissencephaly | A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. |
| DOID:0112234 | microlissencephaly | A lissencephaly characterized by lissencephaly in combination with severe congenital microcephaly. |
| DOID:0112235 | lissencephaly 4 | A microlissencephaly characterized by lissencephaly, severe brain atrophy, extreme microcephaly, and profound intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the NDE1 gene on chromosome 16p13.11. |
11 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050737 | DOID:0112235 |
| is_a | DOID:0112234 | DOID:0112235 |
| is_a | DOID:0050739 | DOID:0112235 |
| is_a | DOID:0080015 | DOID:0112235 |
| is_a | DOID:630 | DOID:0112235 |
| is_a | DOID:863 | DOID:0112235 |
| is_a | DOID:7 | DOID:0112235 |
| is_a | DOID:4 | DOID:0112235 |
| is_a | DOID:0050177 | DOID:0112235 |
| is_a | DOID:0050453 | DOID:0112235 |
| is_a | DOID:2490 | DOID:0112235 |
