Search results for POU1F1

22 hits were found for POU1F1

# Family MCID Name MIFTS Score
1
PTT045 Pituitary Hormone Deficiency, Combined, 1 33 6.312
2
CMB021 Combined Pituitary Hormone Deficiency 37 4.751
3
ISL003 Isolated Growth Hormone Deficiency 55 3.980
4
P HYP083 Hypopituitarism 58 3.939
5
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 3.804
6
P HYP086 Hypothyroidism 64 3.411
7
CRN036 Craniopharyngioma 64 3.411
8
P AXN002 Axenfeld-Rieger Syndrome 53 3.411
9
SPT006 Septooptic Dysplasia 52 3.411
10
PTT037 Pituitary Tumors 48 3.411
11
PTT001 Pituitary Hypoplasia 29 3.411
12
PTT009 Pituitary Gland Disease 56 2.785
13
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 54 2.785
14
BRJ001 Borjeson-Forssman-Lehmann Syndrome 54 2.785
15
PTT041 Pituitary Stalk Interruption Syndrome 47 2.785
16
ANT089 Anti-Pit-1 Antibody Syndrome 11 2.785
17
ISL114 Isolated Growth Hormone Deficiency, Type Ii 45 2.041
18
CMB062 Combined Pituitary Hormone Deficiencies, Genetic Forms 35 2.041
19
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 30 2.041
20
P FRN006 Frontotemporal Dementia 67 0.475
21
GRW007 Growth Hormone Deficiency 51 0.123
22
c CNT101 Central Congenital Hypothyroidism 34 0.087
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