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	meconium aspiration syndrome

Disease ID	564
Disease	meconium aspiration syndrome
Definition	A serious condition in which a newborn breathes a mixture of meconium (the first intestinal discharge) and amniotic fluid into the lungs around the time of delivery. Meconium aspiration syndrome occurs in 5-10 percent of births and typically occurs when the infant is stressed, as when the infant is past its due date.
Synonym	aspiration meconium aspiration meconium syndrome aspiration of meconium aspiration of meconium (disorder) aspiration of meconium -retired- aspiration syndrome, meconium aspiration, meconium mas mas - meconium aspiration syndrome meconium aspiration meconium aspiration nos meconium aspiration syndrome (disorder) meconium aspiration syndrome (finding) meconium aspiration syndrome (finding) [ambiguous] meconium aspiration syndrome [disease/finding] meconium aspiration syndrome nos meconium aspirations meconium inhalation neonatal aspiration of meconium neonatal aspiration of meconium (disorder) of meconium aspiration syndrome, meconium aspiration
Orphanet	ORPHANET:70588
OMIM	OMIM:174800
DOID	DOID:11049
UMLS	C0025048
MeSH	D008471
SNOMED-CT	SNOMEDCT_US_2016_09_01:278927005;SNOMEDCT_US_2016_09_01:206292002
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:9) C0020542 \| pulmonary hypertension \| 3 C0020538 \| hypertension \| 2 C1145670 \| respiratory failure \| 2 C1704437 \| respiratory distress syndrome \| 1 C0035229 \| respiratory insufficiency \| 1 C0011570 \| depression \| 1 C0852283 \| neonatal respiratory distress \| 1 C0004045 \| birth asphyxia \| 1 C0035220 \| neonatal respiratory distress syndrome \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:1) 4142 \| MAS1 \| OMIM
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:38) 9255 \| AIMP1 \| 2.169 \| DISEASES 408 \| ARRB1 \| 1.618 \| DISEASES 551 \| AVP \| 1.174 \| DISEASES 820 \| CAMP \| 1.209 \| DISEASES 388372 \| CCL4L1 \| 2.476 \| DISEASES 9560 \| CCL4L2 \| 1.829 \| DISEASES 1010 \| CDH12 \| 3.092 \| DISEASES 1028 \| CDKN1C \| 1.111 \| DISEASES 1755 \| DMBT1 \| 1.883 \| DISEASES 1906 \| EDN1 \| 3.374 \| DISEASES 2316 \| FLNA \| 1.691 \| DISEASES 2813 \| GP2 \| 1.748 \| DISEASES 3005 \| H1F0 \| 1.312 \| DISEASES 9464 \| HAND2 \| 2.369 \| DISEASES 3055 \| HCK \| 1.37 \| DISEASES 3684 \| ITGAM \| 1.018 \| DISEASES 8972 \| MGAM \| 1.173 \| DISEASES 4295 \| MLN \| 1.244 \| DISEASES 4582 \| MUC1 \| 1.016 \| DISEASES 55922 \| NKRF \| 2.051 \| DISEASES 4843 \| NOS2 \| 1.732 \| DISEASES 4878 \| NPPA \| 1.029 \| DISEASES 55022 \| PID1 \| 2.621 \| DISEASES 8399 \| PLA2G10 \| 4.025 \| DISEASES 5320 \| PLA2G2A \| 3.758 \| DISEASES 5742 \| PTGS1 \| 1.974 \| DISEASES 5799 \| PTPRN2 \| 1.654 \| DISEASES 5817 \| PVR \| 1.641 \| DISEASES 6439 \| SFTPB \| 1.524 \| DISEASES 347734 \| SLC35B2 \| 1.694 \| DISEASES 9300 \| SNORD28 \| 4.264 \| DISEASES 9297 \| SNORD29 \| 3.822 \| DISEASES 26810 \| SNORD41 \| 3.773 \| DISEASES 26806 \| SNORD44 \| 2.892 \| DISEASES 129685 \| TAF8 \| 2.558 \| DISEASES 7124 \| TNF \| 1.98 \| DISEASES 7273 \| TTN \| 4.278 \| DISEASES 9278 \| ZBTB22 \| 1.803 \| DISEASES
Locus	(Waiting for update.)

Disease ID	564
Disease	meconium aspiration syndrome
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:15) HP:0100806 \| Sepsis \| 2 HP:0000822 \| Hypertension \| 2 HP:0002878 \| Respiratory failure \| 2 HP:0002098 \| Respiratory distress \| 2 HP:0002093 \| progressive respiratory failure \| 2 HP:0002092 \| Pulmonary artery hypertension \| 2 HP:0001788 \| Premature rupture of membranes \| 1 HP:0100750 \| Pulmonary atelectasis \| 1 HP:0012758 \| Neurodevelopmental delay \| 1 HP:0002113 \| Pulmonary infiltrates \| 1 HP:0001263 \| Developmental retardation \| 1 HP:0002789 \| Increased respiratory rate or depth of breathing \| 1 HP:0012420 \| Meconium staining of amniotic fluid \| 1 HP:0000716 \| Depression \| 1 HP:0002643 \| Respiratory distress, neonatal \| 1

Disease ID	564
Disease	meconium aspiration syndrome
Manually Symptom	UMLS \| Name(Total Manually Symptoms:7) C2362319 \| acute respiratory distress syndrome (ards) C1963220 \| pulmonary hypertension C1145670 \| respiratory failure C1135361 \| persistent pulmonary hypertension C0032285 \| pneumonitis C0032285 \| lung inflammation C0031190 \| persistent pulmonary hypertension of the newborn
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:5) C0476273 \| respiratory distress \| 2 C1145670 \| respiratory failure \| 2 C0020542 \| pulmonary hypertension \| 2 C0004044 \| asphyxia \| 2 C1135361 \| persistent pulmonary hypertension \| 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:1)
Chr	Pos	SNP_Id	RefGene	EnsemblGene	ENCODE_Factor	ENCODE_TFBS	Chromosome_interaction	GTEx_eQTL	SNP_TFBS_affinity_GWAS3D	SNP_miRNA_target_affinity_PolymiRTS	SNP_splicing_effect_Skippy	SNP_splicing_effect_MutPred_Splice	SNP_ns_protein_effect_dbNSFP	SNP_syn_effect_Silva	SNP_phosphorylation_effect_PhosSNP	PhastCons_score	PhyloP_score	GERP++_RS	Segway_state	Ancestral_allele	ESP_AF	ESP_AFR	ESP_AFR	ESP_EUR	TG_ASN	TG_AMR	TG_AFR	TG_EUR	Type	Consequence	bStatistic	EncH3K27Ac	EncH3K4Me1	EncH3K4Me3	EncNucleo	OMIM	Clinvar
6	160328620	rs220721	NM_002377,MAS1	ENST00000252660,ENSG00000130368	NA	NA	chr6,160320001,160330000,chr1,149820001,149830000,6,Hi-C	NA	LM14,1.3441	LM16,2.8104	LM128,1.4674	LM145,3.5173	LM210,2.9252	NA	NA	NA	NA	NA	NA	0.075	-0.622	-0.631	R5	C	NA	NA	NA	NA	NA	NA	NA	NA	CodingTranscript	SYNONYMOUS	780	3.96	3.00

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	564
Disease	meconium aspiration syndrome
Case	(Waiting for update.)

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