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developmental defect during embryogenesis

Disease Summary
Associated Targets (3534)
Tbio

2610

Tchem

489

Tdark

224

Tclin

211


Explore Associated Targets
Mondo Description A disease that has its basis in the disruption of embryonic morphogenesis.
Mondo Term and Equivalent IDs
MONDO:0019755:  developmental defect during embryogenesis
NCIT:C99267: 
Orphanet:93890: 
SCTID:400038003: 
UMLS:C1302790: 
UMLS:CN206687: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Parents
Tbio

3502

Tchem

731

Tdark

423

Tclin

364

Tbio

2685

Tchem

496

Tdark

238

Tclin

215

Children
Tbio

1111

Tchem

168

Tdark

149

Tclin

47

Tbio

611

Tchem

131

Tclin

46

Tdark

36

Tbio

250

Tchem

45

Tclin

23

Tdark

10

Tbio

199

Tchem

37

Tclin

18

Tdark

6

Tbio

189

Tchem

26

Tclin

21

Tdark

8

Tbio

162

Tchem

37

Tclin

22

Tdark

7

Tbio

111

Tchem

23

Tclin

16

Tdark

3

Tbio

87

Tchem

12

Tclin

4

Tdark

4

Tbio

67

Tchem

23

Tclin

13

Tdark

2

Tbio

67

Tchem

11

Tclin

8

Tbio

42

Tchem

20

Tclin

10

Tdark

1

Tbio

39

Tchem

14

Tclin

6

Tbio

29

Tchem

9

Tclin

6

Tbio

13

Tclin

2

Tchem

1

Tdark

1

Tbio

12

Tclin

1

Tdark

1

Target Novelty (Tin-x)
No novelty measurements found