PedAM
Pediatric Disease Annotations & Medicines
| afibrinogenemia, congenital | ||||
| Disease ID | 1864 |
|---|---|
| Disease | afibrinogenemia, congenital |
| Definition | An inherited blood coagulation disorder characterized by the partial or complete absence of fibrinogen in the blood, resulting in bleeding. |
| Synonym | afibrinogenaemia, congenital afibrinogenaemias, congenital afibrinogenemia, familial afibrinogenemias, congenital afibrinogenemias, familial congenital afibrinogenaemia congenital afibrinogenaemia (disorder) congenital afibrinogenaemias congenital afibrinogenemia congenital afibrinogenemia (disorder) congenital afibrinogenemias congenital hypofibrinogenemia (disorder) congenital hypofibrinogenemias familial afibrinogenemia familial afibrinogenemias hypofibrinogenemia, congenital hypofibrinogenemias, congenital |
| Orphanet | |
| OMIM | |
| DOID | |
| UMLS | C0019250 |
| SNOMED-CT | |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:3) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1864 |
|---|---|
| Disease | afibrinogenemia, congenital |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | (Waiting for update.) |
| Disease ID | 1864 |
|---|---|
| Disease | afibrinogenemia, congenital |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
|---|---|
| (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:1) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0000225 | Gingival bleeding | MP:0005606 | increased bleeding time;HP:0002170 | Intracranial hemorrhage |
Mapped by homologous gene(Total Items:1) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0000007 | Autosomal recessive inheritance | MP:0010659 | abdominal aorta aneurysm;HP:0000140 | Abnormality of the menstrual cycle |
Chemical(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |