ORPHA:695136
Infant-type hemispheric glioma
Synonyms: IHG
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Infant-type hemispheric glioma | IHG |
| fr | Gliome hémisphérique de type infantile | |
| de | Hemisphärisches Gliom vom infantilen Typ | = en |
| es | Glioma hemisférico de tipo infantil | = en |
| it | Glioma emisferico tipo infantile | = en |
| nl | Hemisferisch glioom, zuigeling-type | = en |
| pt | Infant-type hemispheric glioma | |
| pl | Infant-type hemispheric glioma | = en |
| cs | Infant-type hemispheric glioma | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C71.0 | NTBT | attributed | validated |
| ICD-11 | 2A00.0Y | NTBT | attributed | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:251561High-grade astrocytoma
rare neurological diseases; rare neoplastic diseases
4
Genes
0 direct · 6 via subtypesOrphanet records no gene directly on this code.
Recorded by Orphanet on subtypes of this disorder:
| Gene | Subtype | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|---|
| ALK | ORPHA:715697Infant-type hemispheric glioma ALK-altered | Part of a fusion gene in | Assessed | HGNC:427 | ENSG00000171094 | 105590 | 2p23.2-p23.1 | ALK receptor tyrosine kinase | 36910660[PMID]_37000961[PMID]_36996378[PMID] |
| MET | ORPHA:715704Infant-type hemispheric glioma MET-altered | Part of a fusion gene in | Assessed | HGNC:7029 | ENSG00000105976 | 164860 | 7q31.2 | MET proto-oncogene, receptor tyrosine kinase | 38902810[PMID]_31554817(PMID] |
| NTRK1 | ORPHA:715694Infant-type hemispheric glioma NTRK-altered | Part of a fusion gene in | Assessed | HGNC:8031 | ENSG00000198400 | 191315 | 1q23.1 | neurotrophic receptor tyrosine kinase 1 | 36601394[PMID]_31554817[PMID]_35034013[PMID] |
| NTRK2 | ORPHA:715694Infant-type hemispheric glioma NTRK-altered | Part of a fusion gene in | Assessed | HGNC:8032 | ENSG00000148053 | 600456 | 9q21.33 | neurotrophic receptor tyrosine kinase 2 | 36601394[PMID]_31554817[PMID]_35034013[PMID] |
| NTRK3 | ORPHA:715694Infant-type hemispheric glioma NTRK-altered | Part of a fusion gene in | Assessed | HGNC:8033 | ENSG00000140538 | 191316 | 15q25.3 | neurotrophic receptor tyrosine kinase 3 | 36601394[PMID]_31554817[PMID]_35034013[PMID] |
| ROS1 | ORPHA:715701Infant-type hemispheric glioma ROS1-altered | Part of a fusion gene in | Assessed | HGNC:10261 | ENSG00000047936 | 165020 | 6q22.1 | ROS proto-oncogene 1, receptor tyrosine kinase | 36316040[PMID]_35404193[PMID] |
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/695136
- This record as JSON: /data/d/695136.json