Search results for p3h1

Showing 25 of 85 hits for p3h1
# Family MCID Name MIFTS Score
1
c OST118 Osteogenesis Imperfecta, Type Viii 44 66.300
2
BRT054 Brittle Bone Disorder 73 34.844
3
c OST122 Osteogenesis Imperfecta, Type Iii 59 23.042
4
c OST080 Osteogenesis Imperfecta, Type Ii 58 19.266
5
P DNT011 Dentinogenesis Imperfecta 54 10.569
6
P OST002 Osteoporosis 82 10.331
7
P OST135 Osteogenesis Imperfecta, Type I 64 8.664
8
OST015 Osteochondrodysplasia 60 8.664
9
c OST119 Osteogenesis Imperfecta, Type Vii 48 7.999
10
c OST130 Osteogenesis Imperfecta, Type Ix 39 7.864
11
c EHL073 Ehlers-Danlos Syndrome, Classic Type, 1 59 7.474
12
P BRC015 Bruck Syndrome 43 7.474
13
P EHL001 Ehlers-Danlos Syndrome 64 7.474
14
CFF003 Caffey Disease 55 7.305
15
c OST164 Osteoporosis, Juvenile 54 7.305
16
c OST121 Osteogenesis Imperfecta, Type Iv 54 7.305
17
c OST170 Osteogenesis Imperfecta, Type Xix 36 7.305
18
c OST109 Osteogenesis Imperfecta, Type Xiv 37 7.305
19
P KRT014 Keratosis Follicularis Spinulosa Decalvans 35 7.305
20
P CLC057 Cole-Carpenter Syndrome 43 7.305
21
P BND014 Bone Development Disease 31 7.305
22
FBR010 Fibrogenesis Imperfecta Ossium 25 7.305
23
c OST110 Osteogenesis Imperfecta, Type Xv 40 7.305
24
c OST132 Osteogenesis Imperfecta, Type Vi 54 2.231
25
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.625
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