Search results for pou1f1

Showing 25 of 160 hits for pou1f1
# 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
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