Search results for wdr11

#	Family	MCID	Name	MIFTS	Score
1	c	HYP523	Hypogonadotropic Hypogonadism 14 with or Without Anosmia	30	37.559

2	P	KLL001	Kallmann Syndrome	61	24.059

3	P	HYP730	Hypogonadotropic Hypogonadism	60	20.506

4	P	MCR010	Microcephaly	59	20.370

5		GLB002	Glioblastoma	67	14.637

6	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	60	13.834

7		PTT041	Pituitary Stalk Interruption Syndrome	49	9.287

8		NRM018	Normosmic Congenital Hypogonadotropic Hypogonadism	39	8.222

9	P	SNS001	Sensorineural Hearing Loss	59	8.005

10	c	RBN018	Robinow Syndrome, Autosomal Dominant 1	49	7.775

11		ALP097	Alopecia Universalis Congenita	60	7.775

12		CRN288	Corneal Dystrophy, Band-Shaped	37	7.775

13	c	TYP038	Type 1 Diabetes Mellitus 15	31	7.775

14		CYS008	Cystic Echinococcosis	53	7.775

15		LMT001	Limited Scleroderma	50	7.775

16		SBM002	Submandibular Adenitis	17	7.775

17		PRP013	Paraphimosis	29	7.775

18		HYP080	Hypogonadism	51	3.380

19		CHR103	Charge Syndrome	66	2.557

20		ISL004	Isolated Gonadotropin-Releasing Hormone Deficiency	25	1.911

21		CNG562	Congenital Hypogonadotropic Hypogonadism	23	1.773

22		CLP005	Ciliopathy	36	1.654

23	P	GST053	Gastric Cancer	83	1.632

24		AMN001	Amenorrhea	56	1.587

25	P	HRD200	Hereditary Breast Ovarian Cancer Syndrome	70	1.587