Pre-implantation embryo

No Pathway Network information available for Pre-implantation embryo

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

Disorders associated with Pre-implantation embryo SuperPath

according to GeneCards Suite gene sharing
#DisorderTypeGenesScore
1Histiocytoid hemangiomaEnrichmentFOSB, ZFP36L23.75
2Coffin-siris syndrome 1EnrichmentSMARCA4, SOX112.74
3CraniosynostosisEnrichmentSOX11, TFAP2B2.49
4Skin/hair/eye pigmentation, variation in, 8EnrichmentIRF42.37
5Char syndromeEnrichmentTFAP2B2.37
6Oocyte/zygote/embryo maturation arrest 13EnrichmentZFP36L22.37
7Immunodeficiency 131EnrichmentIRF42.37
8Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delayEnrichmentPBX12.37
9Oocyte/zygote/embryo maturation arrest 20EnrichmentMOS2.37
10Lymphedema, primary, with myelodysplasiaEnrichmentGATA22.37
11Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancyEnrichmentNR3C22.37
12Immunodeficiency 21EnrichmentGATA22.37
13Smarca4-deficient sarcoma of thoraxEnrichmentSMARCA42.37
14Ovarian small cell carcinomaEnrichmentSMARCA42.37
15Patent ductus arteriosus 2EnrichmentTFAP2B2.37
16Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadismEnrichmentSOX112.37
17Deafness-lymphedema-leukemia syndromeEnrichmentGATA22.37
18SirenomeliaEnrichmentCDX22.37
19Pseudohyperaldosteronism type 2EnrichmentNR3C22.37
20Breast lobular carcinomaEnrichmentCDH12.37
21Female infertility due to an implantation defect of genetic originEnrichmentZFP36L22.37
22Whipple diseaseEnrichmentIRF42.37
23Anorectal malformationEnrichmentCDX22.37
24Blepharocheilodontic syndrome 1EnrichmentCDH12.07
25Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndromeEnrichmentGATA32.07
26Holoprosencephaly 2EnrichmentSIX32.07
27Ulnar-mammary syndromeEnrichmentTBX32.07
28Rhabdoid tumor predisposition syndrome 2EnrichmentSMARCA42.07
29Pseudohypoaldosteronism, type i, autosomal dominantEnrichmentNR3C22.07
30Hamamy syndromeEnrichmentIRX52.07
31Solitary median maxillary central incisorEnrichmentSIX32.07
32Charcot-marie-tooth disease, axonal, type 2ddEnrichmentATP1A12.07
33Oocyte/zygote/embryo maturation arrest 19EnrichmentNLRP52.07
34Rhabdoid tumor predisposition syndromeEnrichmentSMARCA42.07
35Hypomagnesemia, seizures, and impaired intellectual development 2EnrichmentATP1A12.07
36Choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunctionEnrichmentNKX2-12.07
37Otosclerosis 12EnrichmentSMARCA42.07
38Coffin-siris syndrome 4EnrichmentSMARCA42.07
39B-lymphoblastic leukemia/lymphoma with hyperdiploidyEnrichmentGATA32.07
40Hypoparathyroidism-deafness-renal disease syndromeEnrichmentGATA32.07
41B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)EnrichmentPBX12.07
42Autosomal dominant nonsyndromic deafnessEnrichmentGATA32.07
43Craniofacial dysplasia - osteopenia syndromeEnrichmentIRX52.07
44Renal hypoplasia, bilateralEnrichmentPBX12.07
45Familial patent arterial ductEnrichmentTFAP2B2.07
46PseudohypoaldosteronismEnrichmentNR3C22.07
47Nkx2-1-related disordersEnrichmentNKX2-12.07
48Oocyte/zygote/embryo maturation arrest 16EnrichmentPADI61.89
49Myxoid liposarcomaEnrichmentDDIT31.89
50End stage renal diseaseEnrichmentGATA31.89
51Adenoid cystic carcinomaEnrichmentMYBL11.89
52Chorea, benign hereditaryEnrichmentNKX2-11.77
53Diffuse gastric and lobular breast cancer syndromeEnrichmentCDH11.77
54Microphthalmia, syndromic 3EnrichmentSOX21.77
55SchizencephalyEnrichmentSIX31.77
56Thyroid cancer, nonmedullary, 1EnrichmentNKX2-11.77
57Hereditary ataxiaEnrichmentNKX2-11.77
58Pseudomyogenic hemangioendotheliomaEnrichmentFOSB1.77
59Intestinal pseudo-obstructionEnrichmentTFAP2B1.60
60Cleft lip with or without cleft palateEnrichmentCDH11.60
61Hypothyroidism, congenital, nongoitrous, 2EnrichmentNKX2-11.53
62NeuroblastomaEnrichmentSMARCA41.47
63Choreatic diseaseEnrichmentNKX2-11.47
64Hypogonadotropic hypogonadismEnrichmentSOX111.42
65Ventricular septal defectEnrichmentSMARCA41.42
66Myelodysplastic syndromeEnrichmentGATA21.34
67NanophthalmosEnrichmentSOX21.34
68Atrial heart septal defectEnrichmentSMARCA41.34
69Interatrial communicationEnrichmentSMARCA41.34
70Septooptic dysplasiaEnrichmentSOX21.30
71Hypercholesterolemia, familial, 1EnrichmentSMARCA41.27
72Hypogonadotropic hypogonadism 7 with or without anosmiaEnrichmentSOX111.23
73Cleft lip/palateEnrichmentCDH11.23
74Familial hypercholesterolemiaEnrichmentSMARCA41.21
75Septopreoptic holoprosencephalyEnrichmentSIX31.21
76Midline interhemispheric variant of holoprosencephalyEnrichmentSIX31.21
77Microform holoprosencephalyEnrichmentSIX31.18
78Lobar holoprosencephalyEnrichmentSIX31.18
79Cleft palate, isolatedEnrichmentSMARCA41.15
80Alobar holoprosencephalyEnrichmentSIX31.15
81Semilobar holoprosencephalyEnrichmentSIX31.13
82Autism spectrum disorderEnrichmentNR3C2, PBX11.10
83Macs syndromeEnrichmentSOX21.09
84Endometrial cancerEnrichmentCDH11.06
85MicrophthalmiaEnrichmentSOX21.05
86Inherited cancer-predisposing syndromeEnrichmentCDH1, SMARCA40.96
87Prostate cancerEnrichmentCDH10.93
88Differentiated thyroid carcinomaEnrichmentNKX2-10.93
89CakutEnrichmentGATA30.87
90Cerebral palsyEnrichmentSMARCA40.81
91Leukemia, acute myeloidEnrichmentGATA20.80
92Type 2 diabetes mellitusEnrichmentHMGA10.78
93Gastric cancerEnrichmentCDH10.77
94Hereditary breast carcinomaEnrichmentCDH10.76
95Myeloma, multipleEnrichmentNKX2-10.67
96Breast cancerEnrichmentCDH10.56
97Colorectal cancerEnrichmentCDH10.51
98Ovarian cancerEnrichmentCDH10.45

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