Search results for "craniosynostosis - hydrocephalus - chiari i malformation - radioulnar synostosis"

The MalaCard for "craniosynostosis - hydrocephalus - chiari i malformation - radioulnar synostosis" has been retired.
Searching MalaCards for entries containing "craniosynostosis - hydrocephalus - chiari i malformation - radioulnar synostosis"

52 hits were found for 'craniosynostosis - hydrocephalus - chiari i malformation - radioulnar synostosis'

# Family MCID Name MIFTS Score
1
PLG004 Plagiocephaly 40 0.145
2
P THY032 Thyroiditis 57 0.131
3
c CNG401 Congenital Heart Disease 67 0.103
4
CMP010 Complex Regional Pain Syndrome 59 0.096
5
DYS018 Dysostosis 43 0.094
6
GNG013 Gingivitis 61 0.085
7
P INT068 Intestinal Disease 60 0.085
8
P HYP040 Hypospadias 58 0.080
9
P CRP007 Carpenter Syndrome 49 0.079
10
JCK001 Jackson-Weiss Syndrome 50 0.076
11
P ALG002 Alagille Syndrome 70 0.072
12
P MYC008 Myocarditis 56 0.070
13
INT066 Interstitial Lung Disease 60 0.069
14
END030 End Stage Renal Failure 53 0.065
15
OST017 Osteomyelitis 60 0.064
16
P DDN001 Duodenal Ulcer 51 0.064
17
ORL013 Oral Lichen Planus 53 0.064
18
GST023 Gastric Ulcer 56 0.063
19
ELL001 Ellis-Van Creveld Syndrome 56 0.063
20
c PST041 Posterior Urethral Valves 46 0.062
21
APH001 Aphthous Stomatitis 62 0.062
22
CRT049 Critical Limb Ischemia 51 0.062
23
P ATR005 Atrophic Gastritis 47 0.062
24
KRT001 Keratoconjunctivitis Sicca 58 0.061
25
TYP007 Typhoid Fever 61 0.059
26
RCT015 Reactive Arthritis 65 0.058
27
EXT034 Extrinsic Allergic Alveolitis 58 0.058
28
P EHL015 Ehlers-Danlos Syndrome Progeroid Type 39 0.058
29
CHN016 Cohen Syndrome 55 0.058
30
CHR066 Chronic Fatigue Syndrome 63 0.058
31
P ADL010 Adult Respiratory Distress Syndrome 60 0.057
32
CRD137 Cardiogenic Shock 44 0.057
33
P SMP003 Simpson-Golabi-Behmel Syndrome 46 0.057
34
P AGG001 Aggressive Periodontitis 49 0.057
35
EXT035 Extrinsic Cardiomyopathy 38 0.056
36
P CYS018 Cystitis 54 0.056
37
c JVN010 Juvenile Rheumatoid Arthritis 65 0.056
38
BCT002 Bacterial Vaginosis 53 0.055
39
ANK001 Ankylosis 52 0.055
40
DSS024 Disease of Anatomical Entity 40 0.055
41
FLR002 Filariasis 55 0.054
42
P CRN108 Cranioectodermal Dysplasia 1 48 0.054
43
BNN003 Bone Inflammation Disease 46 0.054
44
DNG001 Dengue Shock Syndrome 41 0.054
45
IDP064 Idiopathic Neutropenia 43 0.054
46
STC004 Stachybotrys Chartarum 38 0.053
47
PPT005 Peptic Ulcer Disease 58 0.052
48
c SBC035 Subacute Cutaneous Lupus Erythematosus 47 0.051
49
NPH004 Nephropathia Epidemica 39 0.050
50
ETH004 Euthyroid Sick Syndrome 37 0.048
51
c PFF007 Pfeiffer Syndrome Type 1 35 0.047
52
MDD010 Middle Ear Disease 47 0.044