Search results for lhx9

56 hits were found for lhx9

# Family MCID Name MIFTS Score
1
GND011 Gonadal Agenesis 20 15.130
2
c 46X082 46,xy Sex Reversal 52 9.429
3
P HYD006 Hydrocephalus 63 1.469
4
OST159 Osteogenic Sarcoma 66 1.387
5
GLM045 Glioma 62 1.323
6
GLL048 Glial Tumor 52 1.323
7
P NRC002 Narcolepsy 55 1.323
8
PNS014 Penis Agenesis 38 1.288
9
P HYP040 Hypospadias 51 1.250
10
P GND004 Gonadal Dysgenesis 46 1.250
11
P BRS047 Breast Cancer 97 0.954
12
IRN008 Iron Overload in Africa 51 0.940
13
RJS001 Ruijs-Aalfs Syndrome 47 0.940
14
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.940
15
HPT079 Hepatoid Adenocarcinoma 39 0.940
16
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.940
17
c HPT073 Hepatitis C Virus 71 0.940
18
P HPT023 Hepatocellular Carcinoma 95 0.940
19
ADL096 Adult Hepatocellular Carcinoma 60 0.940
20
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.940
21
PDT042 Pediatric Hepatocellular Carcinoma 50 0.940
22
PTY007 Pityriasis Rotunda 26 0.940
23
FBR086 Fibrolamellar Carcinoma 59 0.940
24
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.940
25
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.551
26
P MLN008 Melanoma 75 0.551
27
P PNC035 Pancreatic Cancer 86 0.551
28
FRS002 Frasier Syndrome 54 0.309
29
P ALZ034 Alzheimer Disease 87 0.252
30
P FNC044 Fanconi Anemia, Complementation Group C 56 0.178
31
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.178
32
c FNC043 Fanconi Anemia, Complementation Group E 62 0.178
33
c SPR118 Spermatogenic Failure 1 36 0.178
34
c 46X049 46,xy Sex Reversal 2 52 0.178
35
CRV035 Cervical Cancer 72 0.178
36
HLX001 Helix Syndrome 47 0.178
37
P HYP730 Hypogonadotropic Hypogonadism 54 0.178
38
HYP780 Hypoadrenocorticism, Familial 61 0.178
39
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.178
40
P FLL037 Follicular Lymphoma 73 0.178
41
END057 Endometrial Cancer 71 0.178
42
P HNT016 Huntington Disease 73 0.178
43
c 46X055 46,xy Sex Reversal 3 40 0.178
44
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.178
45
c WLM013 Wilms Tumor 1 65 0.178
46
P TTR001 Tetralogy of Fallot 69 0.178
47
P BRC006 Brachydactyly 52 0.178
48
P END044 Endometriosis 62 0.178
49
PTT009 Pituitary Gland Disease 53 0.178
50
HYP080 Hypogonadism 49 0.178
51
CRV002 Cervix Uteri Carcinoma in Situ 48 0.178
52
c 46X011 46, Xy Disorders of Sexual Development 20 0.178
53
CRV045 Cervical Intraepithelial Neoplasia 38 0.178
54
P RTN016 Retinal Degeneration 52 0.178
55
PTT001 Pituitary Hypoplasia 34 0.178
56
PTT041 Pituitary Stalk Interruption Syndrome 54 0.178
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