Search results for FAM20A

39 hits were found for FAM20A

# Family MCID Name MIFTS Score
1
c AML044 Amelogenesis Imperfecta, Type Ig 56 5.536
2
P AML002 Amelogenesis Imperfecta 47 4.872
3
NPH003 Nephrocalcinosis 51 3.757
4
P HYP658 Hypoplastic Amelogenesis Imperfecta 25 2.960
5
GNG012 Gingival Overgrowth 51 2.883
6
P GNG025 Gingival Fibromatosis 51 2.358
7
ACR013 Acrodysostosis 53 2.116
8
HYP021 Hypercementosis 29 2.067
9
TTH002 Tooth Agenesis 61 2.004
10
GNG011 Gingival Disease 44 2.004
11
c CRN243 Carney Complex, Type 1 42 2.004
12
P ACR110 Acrodysostosis 1 with or Without Hormone Resistance 31 2.004
13
SPP003 Suppurative Periapical Periodontitis 31 2.004
14
c PGM021 Pigmented Nodular Adrenocortical Disease, Primary, 1 31 2.004
15
DNT003 Dental Pulp Calcification 28 2.004
16
TTH005 Teeth Hard Tissue Disease 26 2.004
17
SPR019 Superficial Keratitis 23 2.004
18
c MCR282 Microcephaly and Chorioretinopathy 1 18 2.004
19
FBR019 Fibromatosis 44 0.241
20
ATS010 Autosomal Recessive Disease 48 0.171
21
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.132
22
HRW001 Hair Whorl 36 0.132
23
RCK004 Rickets 69 0.108
24
P CRN038 Carney Complex Variant 63 0.108
25
P PRD008 Periodontitis 62 0.108
26
OTT002 Otitis Media 71 0.076
27
MLD001 Melioidosis 67 0.076
28
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.076
29
P HYP069 Hyperparathyroidism 62 0.076
30
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.076
31
OST011 Osteomalacia 52 0.076
32
P AGG001 Aggressive Periodontitis 50 0.076
33
P OVR082 Overgrowth Syndrome 50 0.076
34
HYP017 Hypophosphatemia 49 0.076
35
RTR008 Root Resorption 45 0.076
36
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 45 0.076
37
RNS001 Raine Syndrome 45 0.076
38
c CHR020 Chronic Interstitial Cystitis 37 0.076
39
OBS532 Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type 15 0.076
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