eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| acute myelomonocytic leukemia | ||||
| Disease ID | 1520 |
|---|---|
| Disease | acute myelomonocytic leukemia |
| Definition | A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin. |
| Synonym | [m]acute myelomonocytic leukaemia [m]acute myelomonocytic leukemia acute m4 myeloid leukemia acute myelomonocytic leukaemia acute myelomonocytic leukaemia (clinical) acute myelomonocytic leukaemia, fab m4 acute myelomonocytic leukemia (clinical) acute myelomonocytic leukemia (fab type m4) acute myelomonocytic leukemia (morphologic abnormality) acute myelomonocytic leukemia, fab m4 acute myelomonocytic leukemia, fab m4 (disorder) acute myelomonocytic leukemias amml amml - acute myelomonocytic leukaemia amml - acute myelomonocytic leukemia disorder: acute myelomonocytic leukemia, fab m4 (disorder) fab m4 leukemia myeloid acute m 04 leukemia, acute myelomonocytic leukemia, myeloid, acute, m4 leukemia, myeloid, naegeli-type leukemia, myelomonocytic, acute leukemia, myelomonocytic, acute [disease/finding] leukemia, naegeli-type myeloid leukemias, acute myelomonocytic m4 - acute myelomonocytic leukaemia m4 - acute myelomonocytic leukemia m4 acute myeloid leukemia myeloblastic leukemia myeloid leukemia acute m 04 myeloid leukemia, acute, m4 myeloid leukemia, naegeli type myeloid leukemia, naegeli-type myelomonocytic leukemia, acute myelomonocytic leukemias, acute naegeli-type monocytic leukaemia naegeli-type monocytic leukemia naegeli-type myeloid leukemia |
| Orphanet | |
| UMLS | C0023479 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:15) C0023418 | leukemia | 3 C0024299 | lymphoma | 1 C0013080 | trisomy 21 | 1 C0031485 | phenylketonuria | 1 C0023449 | acute lymphoblastic leukemia | 1 C0015469 | facial nerve paralysis | 1 C0032285 | pneumonia | 1 C1261473 | sarcoma | 1 C0376480 | gingival enlargement | 1 C0022735 | klinefelter's syndrome | 1 C0023434 | chronic lymphocytic leukemia | 1 C0023434 | b-cell chronic lymphocytic leukemia | 1 C0023467 | acute myeloblastic leukemia | 1 C0024291 | hemophagocytic lymphohistiocytosis | 1 C0023448 | lymphoblastic leukemia | 1 |
| 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 | 1520 |
|---|---|
| Disease | acute myelomonocytic leukemia |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:16) HP:0001909 | Leukemia | 3 HP:0002665 | Lymphoma | 1 HP:0001880 | Eosinophilia | 1 HP:0002090 | Pneumonia | 1 HP:0003470 | Inability to move | 1 HP:0030150 | Plasmacytosis | 1 HP:0006721 | Acute lymphocytic leukemia | 1 HP:0004808 | Acute myelogenous leukemia | 1 HP:0000212 | Gingival overgrowth | 1 HP:0001875 | Neutropenia | 1 HP:0010628 | Facial palsy, unilateral or bilateral | 1 HP:0002721 | Immunodeficiency | 1 HP:0002664 | Neoplasia | 1 HP:0004820 | Acute myelomonocytic leukemia | 1 HP:0100242 | Sarcoma | 1 HP:0005550 | Chronic lymphatic leukemia | 1 |
| Disease ID | 1520 |
|---|---|
| Disease | acute myelomonocytic leukemia |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:20) C2707258 | infections C2240374 | eosinophilia C2073625 | pleural effusion C1963154 | renal failure C1963099 | myelodysplasia C1366535 | diabetes insipidus C1333967 | inflammatory pseudotumor of the liver C1332884 | central nervous system leukemia C1136085 | monoclonal gammopathy C0948976 | leukemia cutis C0836924 | thrombocytosis C0684249 | lung cancer C0340968 | pyruvate kinase deficiency C0282548 | leukostasis C0162504 | neutrophilic eccrine hidradenitis C0085077 | sweet's syndrome C0030446 | paralytic ileus C0029166 | oral manifestations C0008626 | chromosomal abnormality C0007965 | chediak-higashi anomaly |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total 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:0) |
|---|
| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
|---|
| (Waiting for update.) |
| Disease ID | 1520 |
|---|---|
| Disease | acute myelomonocytic leukemia |
| Case | (Waiting for update.) |