Search results for ap2m1

Showing 25 of 65 hits for ap2m1
# Family MCID Name MIFTS Score
1
INT387 Intellectual Developmental Disorder, Autosomal Dominant 60, with Seizures 21 34.167
2
P ATS364 Autism 75 20.183
3
EPL230 Epilepsy with Myoclonic-Atonic Seizures 43 10.817
4
c BRC062 Brachydactyly, Type D 37 8.536
5
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 8.536
6
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 45 8.536
7
P DYS005 Dyslexia 40 8.536
8
c HPT001 Hepatitis C 63 1.363
9
c HPT073 Hepatitis C Virus 70 1.363
10
P HPT021 Hepatitis 66 1.363
11
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 40 1.355
12
MDD018 Middle East Respiratory Syndrome 45 1.355
13
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 55 1.241
14
P LNG021 Lung Occult Small Cell Carcinoma 23 1.241
15
LNG019 Lung Combined Type Small Cell Carcinoma 27 1.241
16
P INF037 Inflammatory Bowel Disease 54 1.231
17
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.231
18
P HPT023 Hepatocellular Carcinoma 95 1.167
19
c LKM061 Leukemia, Acute Myeloid 82 1.167
20
VRL011 Viral Infectious Disease 64 1.167
21
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 42 1.167
22
ADR054 Adrenocortical Carcinoma, Hereditary 45 1.130
23
ADN011 Adenoid Cystic Carcinoma 65 1.130
24
ADN018 Adenoma 59 1.130
25
MCP006 Mucoepidermoid Carcinoma 52 1.130
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