Search results for lhx4

37 hits were found for lhx4

# Family MCID Name MIFTS Score
1
PTT044 Pituitary Hormone Deficiency, Combined, 4 28 6.633
2
P HYP083 Hypopituitarism 53 3.723
3
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 3.091
4
PTT001 Pituitary Hypoplasia 34 3.012
5
ISL003 Isolated Growth Hormone Deficiency 49 2.949
6
PTT041 Pituitary Stalk Interruption Syndrome 50 2.913
7
P HYP086 Hypothyroidism 69 2.823
8
c CNG608 Congenital Hypopituitarism 30 2.303
9
PTT045 Pituitary Hormone Deficiency, Combined, 1 36 2.186
10
ACT238 Acth Deficiency, Isolated 52 2.060
11
CMB062 Combined Pituitary Hormone Deficiencies, Genetic Forms 37 2.060
12
c HYP488 Hypothyroidism Due to Deficient Transcription Factors Involved in Pituitary Development or Function 26 2.060
13
P HLP001 Holoprosencephaly 67 1.996
14
SPT006 Septooptic Dysplasia 64 1.996
15
P KLL001 Kallmann Syndrome 61 1.996
16
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.996
17
PTT009 Pituitary Gland Disease 54 1.996
18
BRJ001 Borjeson-Forssman-Lehmann Syndrome 49 1.996
19
GRW007 Growth Hormone Deficiency 46 0.133
21
P LKM062 Leukemia, Acute Lymphoblastic 69 0.109
22
HYP056 Hypoglycemia 66 0.109
23
P CLR023 Colorectal Cancer 99 0.077
24
BRT054 Brittle Bone Disorder 72 0.077
25
P MYP004 Myopathy 70 0.077
26
P LKM002 Leukemia 68 0.077
27
NTR005 Nutritional Deficiency Disease 62 0.077
28
SRC027 Sarcoma, Synovial 58 0.077
29
P STR020 Strabismus 55 0.077
30
c MYP132 Myopathy, Congenital 55 0.077
31
PTH003 Pathologic Nystagmus 52 0.077
32
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 47 0.077
33
DWR001 Dwarfism 44 0.077
34
EMP001 Empty Sella Syndrome 44 0.077
35
MCH006 Mechanical Strabismus 42 0.077
36
P CHR342 Chiari Malformation 41 0.077
37
c CNT101 Central Congenital Hypothyroidism 35 0.077
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