eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| transient hypogammaglobulinemia of infancy | ||||
| Disease ID | 1497 |
|---|---|
| Disease | transient hypogammaglobulinemia of infancy |
| Definition | At birth, newborns are endowed with maternal antibodies. IgG production normally begins at the age of two months. A delay in recovery from this physiological hypogammaglobulinemia between the 3rd and the 6th month of life, and of recovery period between 18 and 36 months defines transient newborn hypogammaglobulinemia. [HPO:probinson] |
| Synonym | immunoglobulin maturational delay thi thi - transient hypogammaglobulinaemia of infancy thi - transient hypogammaglobulinemia of infancy transient hypogammaglobulinaemia of infancy transient hypogammaglobulinemia of infancy (disorder) |
| Orphanet | |
| DOID | |
| ICD10 | |
| UMLS | C0272238 |
| 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:6) |
| Locus | (Waiting for update.) |
| Disease ID | 1497 |
|---|---|
| Disease | transient hypogammaglobulinemia of infancy |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:1) |
| Disease ID | 1497 |
|---|---|
| Disease | transient hypogammaglobulinemia of infancy |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C0014009 | empyema |
| Text Mined Symptom | (Waiting for update.) |
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 | 1497 |
|---|---|
| Disease | transient hypogammaglobulinemia of infancy |
| Case | (Waiting for update.) |