Search results for smad9

#	Family	MCID	Name	MIFTS	Score
1	c	PLM128	Pulmonary Hypertension, Primary, 2	33	39.017

2	P	PLM037	Pulmonary Hypertension	73	11.811

3	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	67	11.281

4	c	PLM164	Pulmonary Hypertension, Primary, 1	76	10.684

5	P	OST002	Osteoporosis	82	10.471

6		HRT015	Heritable Pulmonary Arterial Hypertension	45	10.404

7	c	NRP053	Neuropathy, Hereditary Sensory and Autonomic, Type Iia	69	9.211

8		CLF027	Cleft Palate, Isolated	63	9.211

9		SPN028	Spondyloepimetaphyseal Dysplasia, Strudwick Type	58	9.211

10		CHR619	Chromosome 2q35 Duplication Syndrome	62	9.211

11	P	NRP063	Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive	66	9.211

12	P	DST002	Distal Arthrogryposis	61	9.211

13		PLM184	Pulmonary Arterial Hypertension Associated with Congenital Heart Disease	35	9.043

14	P	ART005	Arteriovenous Malformation	65	6.855

15	P	PLM025	Pulmonary Venoocclusive Disease	48	6.778

16	P	HRD008	Hereditary Hemorrhagic Telangiectasia	64	6.666

17		CRY035	Cryptorchidism, Unilateral or Bilateral	60	6.513

18	P	TTR001	Tetralogy of Fallot	70	6.513

19	P	STR020	Strabismus	57	6.513

20	P	CNR004	Cone-Rod Dystrophy 2	78	6.513

21		EPP022	Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness	35	6.513

22	P	PTN014	Patent Ductus Arteriosus 1	59	6.513

23		CNZ006	Coenzyme Q10 Deficiency, Primary, 1	43	6.513

24	c	CHR641	Charcot-Marie-Tooth Disease, X-Linked Recessive, 2	38	6.513

25	c	CLR134	Ciliary Dyskinesia, Primary, 3	42	6.513