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Hydrops Fetalis
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Disease • C0020305
Definition
A condition characterized by fluid accumulation in two or more anatomic compartments in the fetus. Causes include Rh incompatibility, congenital heart defects, and chromosomal abnormalities.
Synonyms
Hydrops Fetalis • Hydrops fetalis NOS • Fetal Hydrops • Hydrops, Fetal • Fetal Edema • Edema, Fetal • Hydrops Fetalis [Disease/Finding]
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Edema
Mirex
Erythroblastosis, Fetal
alpha-Thalassemia
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Related concepts
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#
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Concept name
|
Type
|
Relation
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Support
|
Score
|
|
1
|
alpha-Thalassemia
|
Disease
|
Known
|
Explain
|
203.38235
|
|
2
|
Mirex
|
Compound
|
Known
|
Explain
|
132.53047
|
|
3
|
Erythroblastosis, Fetal
|
Disease
|
Known
|
Explain
|
132.28835
|
|
4
|
Edema
|
Disease
|
Known
|
Explain
|
25.96910
|
|
5
|
ALPHA-THALASSEMIA MYELODYSPLASIA SYNDROME
|
Disease
|
Inferred
|
Explain
|
19.63936
|
|
6
|
Thalassemia
|
Disease
|
Inferred
|
Explain
|
10.59992
|
|
7
|
HBA2 gene
|
Gene
|
Inferred
|
Explain
|
8.89811
|
|
8
|
HBA1 gene
|
Gene
|
Inferred
|
Explain
|
4.75788
|
|
9
|
Hypoproteinemia
|
Disease
|
Inferred
|
Explain
|
3.52625
|
|
10
|
Kernicterus
|
Disease
|
Inferred
|
Explain
|
2.15546
|
|
11
|
Blood Group Incompatibility
|
Disease
|
Inferred
|
Explain
|
2.06846
|
|
12
|
Fetal Diseases
|
Disease
|
Inferred
|
Explain
|
2.04899
|
|
13
|
Hypoglycemia
|
Disease
|
Inferred
|
Explain
|
1.86948
|
|
14
|
Hyperlipidemia
|
Disease
|
Inferred
|
Explain
|
1.39121
|
|
15
|
Cataract
|
Other
|
Inferred
|
Explain
|
1.39057
|
|
16
|
ATRX gene
|
Gene
|
Inferred
|
Explain
|
1.24492
|
|
17
|
Hydrocarbons, Chlorinated
|
Compound
|
Inferred
|
Explain
|
0.78916
|
|
18
|
Malignant neoplasm of skin
|
Disease
|
Inferred
|
Explain
|
0.77088
|
|
19
|
Neonatal disorder
|
Disease
|
Inferred
|
Explain
|
0.62426
|
|
20
|
Malignant Neoplasms
|
Disease
|
Inferred
|
Explain
|
0.40590
|
|
21
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MIR144 gene
|
Gene
|
Inferred
|
Explain
|
0.11403
|
|
22
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Hemoglobinopathies
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Disease
|
Inferred
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Explain
|
0.11084
|
|
23
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AR gene
|
Gene
|
Inferred
|
Explain
|
0.10979
|
|
24
|
Fetal Hypoxia
|
Disease
|
Inferred
|
Explain
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0.10973
|
|
25
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HBB gene
|
Gene
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Inferred
|
Explain
|
0.10186
|
|
26
|
beta Thalassemia
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Disease
|
Inferred
|
Explain
|
0.09999
|
|
27
|
Hypoalbuminemia
|
Disease
|
Inferred
|
Explain
|
0.09885
|
|
28
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HYPOPROTEINEMIA, HYPERCATABOLIC
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Disease
|
Inferred
|
Explain
|
0.08822
|
|
29
|
Chorioamnionitis
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Disease
|
Inferred
|
Explain
|
0.08585
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|
30
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Fetal Macrosomia
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Disease
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Inferred
|
Explain
|
0.07922
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|
31
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Nuchal Cord
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Disease
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Inferred
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Explain
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0.07425
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|
32
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
|
Disease
|
Inferred
|
Explain
|
0.07372
|
|
33
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Fetal Nutrition Disorders
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Disease
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Inferred
|
Explain
|
0.07091
|
|
34
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Meconium Aspiration Syndrome
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Disease
|
Inferred
|
Explain
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0.07069
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|
35
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Anemia, Hemolytic, Congenital
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Disease
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Inferred
|
Explain
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0.06366
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|
36
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Fetal Alcohol Syndrome
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Disease
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Inferred
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Explain
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0.06194
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|
37
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Rh Isoimmunization
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Disease
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Inferred
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Explain
|
0.05829
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|
38
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Pregnancy Complications
|
Disease
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Inferred
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Explain
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0.05510
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|
39
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HEINZ BODY ANEMIAS
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Disease
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Inferred
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Explain
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0.05094
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|
40
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Fetal Growth Retardation
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Disease
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Inferred
|
Explain
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0.05055
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|
41
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Blood Protein Disorders
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Disease
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Inferred
|
Explain
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0.04206
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|
42
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Furosemide
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Compound
|
Inferred
|
Explain
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0.03916
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|
43
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Hematological Disease
|
Disease
|
Inferred
|
Explain
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0.03799
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|
44
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Anoxia
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Disease
|
Inferred
|
Explain
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0.03424
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|
45
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Immune System Diseases
|
Disease
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Inferred
|
Explain
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0.03350
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|
46
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Hyperbilirubinemia
|
Disease
|
Inferred
|
Explain
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0.02564
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|
47
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Methyl Methanesulfonate
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Compound
|
Inferred
|
Explain
|
0.02532
|
|
48
|
Cooley's anemia
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Disease
|
Inferred
|
Explain
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0.02511
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|
49
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TZI 41127
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Compound
|
Inferred
|
Explain
|
0.02403
|
|
50
|
BN 50739
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Compound
|
Inferred
|
Explain
|
0.02377
|
|
51
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AHSP gene
|
Gene
|
Inferred
|
Explain
|
0.02351
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|
52
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sinapinic acid
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Compound
|
Inferred
|
Explain
|
0.02347
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|
53
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cyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl ester
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Compound
|
Inferred
|
Explain
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0.02282
|
|
54
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Brain Diseases, Metabolic
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Disease
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Inferred
|
Explain
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0.02263
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|
55
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ATAXIA, EARLY-ONSET, WITH OCULOMOTOR APRAXIA AND HYPOALBUMINEMIA
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Disease
|
Inferred
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Explain
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0.02212
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|
56
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Placenta Disorders
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Disease
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Inferred
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Explain
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0.02176
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57
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Cromoglycate
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Compound
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Inferred
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Explain
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0.02167
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|
58
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PEHO syndrome
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Disease
|
Inferred
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Explain
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0.02167
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|
59
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Flexidol
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Compound
|
Inferred
|
Explain
|
0.02091
|
|
60
|
Sodium Meclofenamate
|
Compound
|
Inferred
|
Explain
|
0.02067
|
|
61
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12-(acetyloxy)-4,4,8-trimethylhomoandrost-16-ene-17,17a-dicarboxaldehyde
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Compound
|
Inferred
|
Explain
|
0.02051
|
|
62
|
1-(4-(benzothiazol-2-yloxy)benzyl)piperidine-4-carboxylic acid
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Compound
|
Inferred
|
Explain
|
0.02040
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|
63
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2-(3-methoxy-4-(4-chlorophenylthioethoxy)-5-(N-methyl-N-hydroxyureidyl)methylphenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran
|
Compound
|
Inferred
|
Explain
|
0.02040
|
|
64
|
AA 861
|
Compound
|
Inferred
|
Explain
|
0.01971
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|
65
|
phenidone
|
Compound
|
Inferred
|
Explain
|
0.01953
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|
66
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Edema, Cardiac
|
Disease
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Inferred
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Explain
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0.01930
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|
67
|
Methylnitrosourea
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Compound
|
Inferred
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Explain
|
0.01811
|
|
68
|
thioperamide
|
Compound
|
Inferred
|
Explain
|
0.01795
|
|
69
|
HBE1 gene
|
Gene
|
Inferred
|
Explain
|
0.01579
|
|
70
|
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS
|
Disease
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Inferred
|
Explain
|
0.01578
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|
71
|
Fetal Membranes, Premature Rupture
|
Disease
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Inferred
|
Explain
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0.01554
|
|
72
|
Isopromethazine
|
Compound
|
Inferred
|
Explain
|
0.01548
|
|
73
|
Methysergide
|
Compound
|
Inferred
|
Explain
|
0.01528
|
|
74
|
Chloracne
|
Disease
|
Inferred
|
Explain
|
0.01496
|
|
75
|
Carrageenan
|
Compound
|
Inferred
|
Explain
|
0.01475
|
|
76
|
Inflammation
|
Disease
|
Inferred
|
Explain
|
0.01458
|
|
77
|
BAY u 3406
|
Compound
|
Inferred
|
Explain
|
0.01457
|
|
78
|
Mangifera indica extract
|
Compound
|
Inferred
|
Explain
|
0.01457
|
|
79
|
Hemoglobin C Disease
|
Disease
|
Inferred
|
Explain
|
0.01380
|
|
80
|
KEGG:hsa05143
|
Pathway
|
Inferred
|
Explain
|
0.01345
|
|
81
|
perfluorooctanoic acid
|
Compound
|
Inferred
|
Explain
|
0.01207
|
|
82
|
Sodium Salicylate
|
Compound
|
Inferred
|
Explain
|
0.01182
|
|
83
|
Phenylbutazone
|
Compound
|
Inferred
|
Explain
|
0.01163
|
|
84
|
L 660,711
|
Compound
|
Inferred
|
Explain
|
0.01125
|
|
85
|
Crotalid Venoms
|
Compound
|
Inferred
|
Explain
|
0.01089
|
|
86
|
CPM gene
|
Gene
|
Inferred
|
Explain
|
0.01085
|
|
87
|
KEGG:hsa05144
|
Pathway
|
Inferred
|
Explain
|
0.01033
|
|
88
|
L 663536
|
Compound
|
Inferred
|
Explain
|
0.00991
|
|
89
|
bis(4-hydroxycinnamoyl)methane
|
Compound
|
Inferred
|
Explain
|
0.00989
|
|
90
|
Ketoprofen
|
Compound
|
Inferred
|
Explain
|
0.00980
|
|
91
|
demethoxycurcumin
|
Compound
|
Inferred
|
Explain
|
0.00978
|
|
92
|
Persistent Hyperinsulinemia Hypoglycemia of Infancy
|
Disease
|
Inferred
|
Explain
|
0.00974
|
|
93
|
captafol
|
Compound
|
Inferred
|
Explain
|
0.00966
|
|
94
|
Piroxicam
|
Compound
|
Inferred
|
Explain
|
0.00953
|
|
95
|
SLC9A2 gene
|
Gene
|
Inferred
|
Explain
|
0.00936
|
|
96
|
Insulin Coma
|
Disease
|
Inferred
|
Explain
|
0.00928
|
|
97
|
Signs and Symptoms
|
Disease
|
Inferred
|
Explain
|
0.00912
|
|
98
|
Hypoglycemia, leucine-induced
|
Disease
|
Inferred
|
Explain
|
0.00908
|
|
99
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Pregnancy in Diabetics
|
Disease
|
Inferred
|
Explain
|
0.00875
|
|
100
|
Anafranil
|
Compound
|
Inferred
|
Explain
|
0.00864
|
|