| # |
|
Family |
MCID |
Name |
MIFTS |
Score |
| 1 |
|
|
PTT070 |
Pituitary Hormone Deficiency, Combined or Isolated, 1 |
35 |
42.704 |
|
| 2 |
|
|
HYP083 |
Hypopituitarism |
54 |
18.884 |
|
|
| 3 |
|
|
PTT046 |
Pituitary Hormone Deficiency, Combined, 2 |
63 |
17.763 |
|
|
| 4 |
|
|
ISL114 |
Isolated Growth Hormone Deficiency, Type Ii |
44 |
15.991 |
|
|
| 5 |
|
P
|
HYP086 |
Hypothyroidism |
68 |
15.816 |
|
|
| 6 |
|
|
PTT001 |
Pituitary Hypoplasia |
31 |
15.238 |
|
|
| 7 |
|
c
|
CNG006 |
Congenital Hypothyroidism |
64 |
14.830 |
|
|
| 8 |
|
P
|
PTT006 |
Pituitary Adenoma |
50 |
13.806 |
|
|
| 9 |
|
|
ADN018 |
Adenoma |
59 |
13.789 |
|
|
| 10 |
|
|
PRL009 |
Prolactinoma |
63 |
13.544 |
|
|
| 11 |
|
|
CMB062 |
Combined Pituitary Hormone Deficiencies, Genetic Forms |
51 |
13.427 |
|
|
| 12 |
|
|
ISL003 |
Isolated Growth Hormone Deficiency |
50 |
12.722 |
|
|
| 13 |
|
|
SPT006 |
Septooptic Dysplasia |
65 |
10.873 |
|
|
| 14 |
|
|
CRN036 |
Craniopharyngioma |
62 |
10.425 |
|
|
| 15 |
|
|
STS002 |
Situs Inversus |
52 |
10.425 |
|
|
| 16 |
|
|
EMP001 |
Empty Sella Syndrome |
42 |
10.218 |
|
|
| 17 |
|
|
PTT009 |
Pituitary Gland Disease |
53 |
9.008 |
|
|
| 18 |
|
c
|
HYP795 |
Hypothyroidism, Congenital, Nongoitrous, 4 |
53 |
8.613 |
|
|
| 19 |
|
c
|
HYP488 |
Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function |
28 |
8.558 |
|
|
| 20 |
|
P
|
HLP001 |
Holoprosencephaly |
66 |
8.382 |
|
|
| 21 |
|
|
ACT238 |
Acth Deficiency, Isolated |
53 |
7.432 |
|
|
| 22 |
|
|
SHH001 |
Sheehan Syndrome |
47 |
7.432 |
|
|
| 23 |
|
|
HYP856 |
Hypothyroidism, Central, with Testicular Enlargement |
37 |
7.372 |
|
|
| 24 |
|
|
ADP001 |
Adiposis Dolorosa |
46 |
7.225 |
|
|
| 25 |
|
c
|
CNG031 |
Congenital Nervous System Abnormality |
32 |
7.225 |
|
|
