Search results for PRIMPOL

23 hits were found for PRIMPOL

# Family MCID Name MIFTS Score
1
P MYP006 Myopia 55 5.278
2
c MYP075 Myopia 22, Autosomal Dominant 17 4.424
3
XRD010 Xeroderma Pigmentosum, Variant Type 73 3.082
4
c FNC027 Fanconi Anemia, Complementation Group a 81 3.028
5
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 46 3.028
6
RFR003 Refractive Error 43 3.028
7
c MTC065 Mitochondrial Dna Depletion Syndrome 8a 41 3.028
8
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 59 2.141
9
c MTC061 Mitochondrial Dna Depletion Syndrome 1 48 2.141
10
c MTC062 Mitochondrial Dna Depletion Syndrome 2 44 2.141
11
c MTC078 Mitochondrial Dna Depletion Syndrome 11 37 2.141
12
c MTC126 Mitochondrial Dna Depletion Syndrome 14 31 2.141
13
c CHR700 Charcot-Marie-Tooth Disease Type 2a2b 17 2.141
14
WRN001 Werner Syndrome 69 0.086
15
OST159 Osteogenic Sarcoma 66 0.086
16
KRN002 Kearns-Sayre Syndrome 63 0.086
17
P MTC069 Mitochondrial Disorders 56 0.086
18
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 55 0.086
19
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 54 0.086
20
P PTS002 Ptosis 53 0.086
21
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 50 0.086
22
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.086
23
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.086
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