Search results for zbtb18

#	Family	MCID	Name	MIFTS	Score
1	c	INT513	Intellectual Developmental Disorder, Autosomal Dominant 22	36	46.456

2	P	MCR010	Microcephaly	59	14.476

3	c	RTN114	Retinitis Pigmentosa 58	34	9.848

4	c	CNG513	Congenital Ptosis	51	7.999

5		CHR582	Chromosome 3q29 Duplication Syndrome	33	7.999

6	c	DVL078	Developmental and Epileptic Encephalopathy 54	36	7.999

7	c	CNG031	Congenital Nervous System Abnormality	32	7.999

8		BRT005	Barth Syndrome	57	7.999

9	c	DVL053	Developmental and Epileptic Encephalopathy 27	38	7.999

10		TRN017	Transient Neonatal Neutropenia	13	7.999

11		TRN013	Transient Neonatal Thrombocytopenia	18	7.999

12		GLB002	Glioblastoma	67	2.663

13		HYP265	Hypotonia	46	2.157

14		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	46	1.697

15		CRP032	Corpus Callosum, Agenesis of	55	1.324

16	P	HPT023	Hepatocellular Carcinoma	96	1.257

17		CHR662	Chromosome 15q13.3 Deletion Syndrome	41	1.257

18	P	SYN057	Syndromic Intellectual Disability	33	1.257

19	c	HNR003	Hnrnpu-Related Neurodevelopmental Disorder	11	1.257

20	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	1.178

21	P	BRS047	Breast Cancer	97	0.712

22		BRK010	Burkitt Lymphoma	67	0.503

23	P	PNC035	Pancreatic Cancer	91	0.503

24	P	GLM040	Glioma Susceptibility 1	71	0.503

25	P	OVR042	Ovarian Cancer	89	0.503

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