PedAM
Pediatric Disease Annotations & Medicines
| ulnar neuropathy | ||||
| Disease ID | 1842 |
|---|---|
| Disease | ulnar neuropathy |
| Definition | Disease involving the ULNAR NERVE from its origin in the BRACHIAL PLEXUS to its termination in the hand. Clinical manifestations may include PARESIS or PARALYSIS of wrist flexion, finger flexion, thumb adduction, finger abduction, and finger adduction. Sensation over the medial palm, fifth finger, and ulnar aspect of the ring finger may also be impaired. Common sites of injury include the AXILLA, cubital tunnel at the ELBOW, and Guyon's canal at the wrist. (From Joynt, Clinical Neurology, 1995, Ch51 pp43-5) |
| Synonym | nerve disease, ulnar nerve diseases, ulnar neuropathies, ulnar neuropathy ulnar neuropathy, ulnar ulnar nerve dis ulnar nerve disease ulnar nerve diseases ulnar neuropathies ulnar neuropathies [disease/finding] ulnar neuropathy (disorder) ulnar neuropathy (disorder) [ambiguous] |
| DOID | |
| UMLS | C0154743 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:3) |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:28) 8935 | SKAP2 | DISEASES 8050 | PDHX | DISEASES 6521 | SLC4A1 | DISEASES 25939 | SAMHD1 | DISEASES 4854 | NOTCH3 | DISEASES 5276 | SERPINI2 | DISEASES 150094 | SIK1 | DISEASES 4851 | NOTCH1 | DISEASES 1737 | DLAT | DISEASES 5805 | PTS | DISEASES 6051 | RNPEP | DISEASES 23588 | KLHDC2 | DISEASES 5376 | PMP22 | DISEASES 923 | CD6 | DISEASES 9939 | RBM8A | DISEASES 114548 | NLRP3 | DISEASES 9639 | ARHGEF10 | DISEASES 23764 | MAFF | DISEASES 1861 | TOR1A | DISEASES 23644 | EDC4 | DISEASES 2157 | F8 | DISEASES 4153 | MBL2 | DISEASES 4855 | NOTCH4 | DISEASES 2591 | GALNT3 | DISEASES 654364 | NME1-NME2 | DISEASES 54900 | LAX1 | DISEASES 101 | ADAM8 | DISEASES 820 | CAMP | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1842 |
|---|---|
| Disease | ulnar neuropathy |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:2) |
| Disease ID | 1842 |
|---|---|
| Disease | ulnar neuropathy |
| 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) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (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:1) | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
| C0154743 | phenytoin | D010672 | 57-41-0 | ulnar neuropathies | MESH:D020424 | marker/mechanism | 4365396 | ||
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.) | |