Search results for lhx9

54 hits were found for lhx9

# Family MCID Name MIFTS Score
1
GND011 Gonadal Agenesis 20 16.513
2
ADR049 Adrenal Hypoplasia, Congenital 53 9.135
3
c 46X082 46,xy Sex Reversal 52 9.135
4
P HYD006 Hydrocephalus 61 3.348
5
OST159 Osteogenic Sarcoma 66 3.014
6
P NRC002 Narcolepsy 56 2.759
7
GLL048 Glial Tumor 52 2.759
8
GLM045 Glioma 63 2.759
9
PNS014 Penis Agenesis 36 2.617
10
P HYP040 Hypospadias 51 2.463
11
P GND004 Gonadal Dysgenesis 47 2.463
12
FRS002 Frasier Syndrome 54 1.248
13
P BRS047 Breast Cancer 98 0.954
14
IRN008 Iron Overload in Africa 51 0.938
15
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.938
16
HPT079 Hepatoid Adenocarcinoma 39 0.938
17
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.938
18
RJS001 Ruijs-Aalfs Syndrome 47 0.938
19
c HPT073 Hepatitis C Virus 71 0.938
20
P HPT023 Hepatocellular Carcinoma 96 0.938
21
PDT042 Pediatric Hepatocellular Carcinoma 49 0.938
22
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.938
23
ADL096 Adult Hepatocellular Carcinoma 60 0.938
24
FBR086 Fibrolamellar Carcinoma 59 0.938
25
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.938
26
PTY007 Pityriasis Rotunda 26 0.938
27
P ALZ034 Alzheimer Disease 87 0.721
28
c 46X049 46,xy Sex Reversal 2 49 0.721
29
CRV035 Cervical Cancer 73 0.721
30
END057 Endometrial Cancer 72 0.721
31
P BRC006 Brachydactyly 51 0.721
32
c FNC043 Fanconi Anemia, Complementation Group E 62 0.721
33
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.721
34
P FNC044 Fanconi Anemia, Complementation Group C 56 0.721
35
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.721
36
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.721
37
HYP780 Hypoadrenocorticism, Familial 61 0.721
38
c WLM013 Wilms Tumor 1 66 0.721
39
P TTR001 Tetralogy of Fallot 69 0.721
40
P HNT016 Huntington Disease 73 0.721
41
P FLL037 Follicular Lymphoma 74 0.721
42
P HYP730 Hypogonadotropic Hypogonadism 53 0.721
43
CRV002 Cervix Uteri Carcinoma in Situ 47 0.721
44
P RTN016 Retinal Degeneration 52 0.721
45
HLX001 Helix Syndrome 48 0.721
46
P END044 Endometriosis 62 0.721
47
PTT001 Pituitary Hypoplasia 34 0.721
48
HYP080 Hypogonadism 50 0.721
49
c 46X011 46, Xy Disorders of Sexual Development 20 0.721
50
PTT041 Pituitary Stalk Interruption Syndrome 54 0.721
51
CRV045 Cervical Intraepithelial Neoplasia 39 0.721
52
P PNC035 Pancreatic Cancer 86 0.551
53
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.551
54
P MLN008 Melanoma 76 0.551
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