Search results for hesx1

30 hits were found for hesx1

# Family MCID Name MIFTS Score
1
SPT006 Septooptic Dysplasia 52 7.720
2
GRW007 Growth Hormone Deficiency 51 4.686
3
CMB021 Combined Pituitary Hormone Deficiency 37 4.469
4
P KLL001 Kallmann Syndrome 63 4.344
5
PTT045 Pituitary Hormone Deficiency, Combined, 1 33 4.283
6
P HYP083 Hypopituitarism 58 4.012
7
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 3.546
8
PTT041 Pituitary Stalk Interruption Syndrome 47 3.407
9
PTT001 Pituitary Hypoplasia 29 3.334
10
P HYP086 Hypothyroidism 64 3.291
11
PTT009 Pituitary Gland Disease 56 3.291
12
ISL003 Isolated Growth Hormone Deficiency 55 3.291
13
P SCH018 Schizencephaly 52 2.738
14
BRJ001 Borjeson-Forssman-Lehmann Syndrome 54 2.687
15
c AXN009 Axenfeld-Rieger Syndrome, Type 1 46 2.687
16
FRY006 Fryns Microphthalmia Syndrome 45 2.687
17
ISL114 Isolated Growth Hormone Deficiency, Type Ii 45 2.687
18
ISL115 Isolated Growth Hormone Deficiency, Type Iii 41 2.687
19
ADM001 Adamantinous Craniopharyngioma 26 2.687
20
CNT043 Central Nervous System Organ Benign Neoplasm 23 2.687
21
CMB062 Combined Pituitary Hormone Deficiencies, Genetic Forms 35 1.967
22
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 30 1.967
23
c SYS001 Systemic Lupus Erythematosus 86 0.080
24
P INF038 Influenza 76 0.080
25
ADN018 Adenoma 63 0.080
26
P PTT006 Pituitary Adenoma 52 0.080
27
P OPT070 Optic Nerve Hypoplasia, Bilateral 43 0.080
28
CRB009 Cerebritis 41 0.080
29
c CNT101 Central Congenital Hypothyroidism 34 0.080
30
SPT019 Septo-Optic Dysplasia Spectrum 28 0.080
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