PedAM

Pediatric Disease Annotations & Medicines


	milk allergy

Disease ID	1461
Disease	milk allergy
Definition	Allergic reaction to milk (usually cow's milk) or milk products. MILK HYPERSENSITIVITY should be differentiated from LACTOSE INTOLERANCE, an intolerance to milk as a result of congenital deficiency of lactase.
Synonym	allergies food milk allergies milk allergies, milk allergy milk allergy, milk hypersensitivities, milk hypersensitivity, milk milk allergies milk food allergy milk hypersensitivities milk hypersensitivity milk hypersensitivity [disease/finding]
DOID	DOID:4376
UMLS	C0079840
MeSH	D016269
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:21) C0011615 \| atopic dermatitis \| 4 C0011603 \| dermatitis \| 3 C0004096 \| asthma \| 2 C0017168 \| esophageal reflux \| 2 C0017168 \| gastroesophageal reflux disease \| 2 C0017168 \| esophageal reflux disease \| 2 C0017168 \| gastroesophageal reflux \| 2 C0017168 \| oesophageal reflux \| 2 C0024523 \| malabsorption \| 1 C0017160 \| gastroenteritis \| 1 C0001339 \| acute pancreatitis \| 1 C0014544 \| epileptic seizures \| 1 C0024523 \| intestinal malabsorption \| 1 C1262481 \| eosinophilic gastroenteritis \| 1 C0004096 \| bronchial asthma \| 1 C0033246 \| proctitis \| 1 C0014544 \| epileptic seizure \| 1 C0026769 \| multiple sclerosis \| 1 C0037199 \| sinusitis \| 1 C0009806 \| constipation \| 1 C0019569 \| hirschsprung's disease \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) FAM117A \| 81558 \| GWASCAT
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:66) 51087 \| YBX2 \| DISEASES 30009 \| TBX21 \| DISEASES 7040 \| TGFB1 \| DISEASES 973 \| CD79A \| DISEASES 969 \| CD69 \| DISEASES 3458 \| IFNG \| DISEASES 3565 \| IL4 \| DISEASES 3567 \| IL5 \| DISEASES 6402 \| SELL \| DISEASES 51119 \| SBDS \| DISEASES 1446 \| CSN1S1 \| DISEASES 79132 \| DHX58 \| DISEASES 51124 \| IER3IP1 \| DISEASES 9883 \| POM121 \| DISEASES 967 \| CD63 \| DISEASES 27429 \| HTRA2 \| DISEASES 3569 \| IL6 \| DISEASES 3682 \| ITGAE \| DISEASES 3938 \| LCT \| DISEASES 2206 \| MS4A2 \| DISEASES 55364 \| IMPACT \| DISEASES 115650 \| TNFRSF13C \| DISEASES 23528 \| ZNF281 \| DISEASES 213 \| ALB \| DISEASES 3906 \| LALBA \| DISEASES 6356 \| CCL11 \| DISEASES 6037 \| RNASE3 \| DISEASES 3603 \| IL16 \| DISEASES 6036 \| RNASE2 \| DISEASES 1673 \| DEFB4A \| DISEASES 1448 \| CSN3 \| DISEASES 3596 \| IL13 \| DISEASES 3575 \| IL7R \| DISEASES 6373 \| CXCL11 \| DISEASES 131450 \| CD200R1 \| DISEASES 3563 \| IL3RA \| DISEASES 5155 \| PDGFB \| DISEASES 85480 \| TSLP \| DISEASES 1447 \| CSN2 \| DISEASES 921 \| CD5 \| DISEASES 5265 \| SERPINA1 \| DISEASES 5169 \| ENPP3 \| DISEASES 11005 \| SPINK5 \| DISEASES 2673 \| GFPT1 \| DISEASES 83881 \| MIXL1 \| DISEASES 7042 \| TGFB2 \| DISEASES 4720 \| NDUFS2 \| DISEASES 632 \| BGLAP \| DISEASES 7062 \| TCHH \| DISEASES 959 \| CD40LG \| DISEASES 292 \| SLC25A5 \| DISEASES 50943 \| FOXP3 \| DISEASES 2625 \| GATA3 \| DISEASES 9350 \| CER1 \| DISEASES 9189 \| ZBED1 \| DISEASES 10333 \| TLR6 \| DISEASES 1621 \| DBH \| DISEASES 4773 \| NFATC2 \| DISEASES 7124 \| TNF \| DISEASES 3586 \| IL10 \| DISEASES 4700 \| NDUFA6 \| DISEASES 100289462 \| DEFB4B \| DISEASES 26298 \| EHF \| DISEASES 930 \| CD19 \| DISEASES 3684 \| ITGAM \| DISEASES 387521 \| TMEM189 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1461
Disease	milk allergy
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:15) HP:0001047 \| Atopic dermatitis \| 4 HP:0002099 \| Asthma \| 2 HP:0002020 \| Heartburn \| 2 HP:0012450 \| Chronic constipation \| 1 HP:0000246 \| Sinus inflammation \| 1 HP:0002024 \| Intestinal malabsorption \| 1 HP:0002019 \| Dyschezia \| 1 HP:0002315 \| Headaches \| 1 HP:0001250 \| Seizures \| 1 HP:0100845 \| Anaphylactic shock \| 1 HP:0001735 \| Acute pancreatitis \| 1 HP:0002584 \| Intestinal hemorrhage \| 1 HP:0002566 \| Intestinal malrotation \| 1 HP:0011109 \| Chronic sinusitis \| 1 HP:0004387 \| Enterocolitis \| 1

Disease ID	1461
Disease	milk allergy
Manually Symptom	(Waiting for update.)
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:2) C0001339 \| acute pancreatitis \| 1 C0267373 \| intestinal bleeding \| 1

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:1)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs9898058	25710614	81558	FAM117A	umls:C0079840	GWASCAT	Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.	0.12	2015	FAM117A	17	49741459	C	T

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.)

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.)

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