PedAM
Pediatric Disease Annotations & Medicines
| chiari malformation type ii | ||||
| Disease ID | 1967 |
|---|---|
| Disease | chiari malformation type ii |
| Synonym | arnold chiari malformation, type 2 arnold chiari malformation, type ii arnold chiari type 2 arnold-chiari malformation, type 2 arnold-chiari malformation, type ii arnold-chiari syndrome, type ii chiari malformation type 2 chiari malformation type ii (disorder) chiari malformation, type ii type ii arnold chiari malformation type ii arnold-chiari malformation |
| OMIM | |
| UMLS | C0555206 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:5) C0037315 | sleep apnea | 1 C0020255 | hydrocephalus | 1 C0080178 | spinal dysraphism | 1 C0026985 | myelodysplasia | 1 C0037315 | sleep-disordered breathing | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1967 |
|---|---|
| Disease | chiari malformation type ii |
| Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:17) HP:0003690 | Limb weakness HP:0000639 | Nystagmus HP:0002483 | Bulbar signs HP:0002308 | Chiari malformation HP:0001251 | Ataxia HP:0002318 | Cervical myelopathy HP:0012318 | Occipital neuralgia HP:0011968 | Feeding difficulties HP:0001274 | Absent corpus callosum HP:0002179 | Opisthotonus HP:0001252 | Hypotonia HP:0000961 | Cyanosis HP:0005348 | Inspiratory stridor HP:0002414 | Spina bifida HP:0000238 | Nonsyndromal hydrocephalus HP:0002282 | Heterotopias HP:0002015 | Swallowing difficulty |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:6) |
| Disease ID | 1967 |
|---|---|
| Disease | chiari malformation type ii |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |