9625
(4.0%)

DECIPHER:278349

Primary amenorrhea

9625
(4.0%)

MyGene2:259

Hearing impairment

9625
(4.0%)

DECIPHER:257588

Strabismus

9625
(4.0%)

DECIPHER:273901

Esotropia

9625
(4.0%)

MyGene2:351

Vesicoureteral reflux

9625
(4.0%)

UDN:050

Optic atrophy

9625
(4.0%)

MyGene2:71

Strabismus

9625
(4.0%)

MyGene2:2154

Strabismus

9625
(4.0%)

MyGene2:160

Ptosis

9625
(4.0%)

DECIPHER:269533

Ataxia

9625
(4.0%)

MyGene2:2105

Cryptorchidism

9625
(4.0%)

MyGene2:2106

Cryptorchidism

9625
(4.0%)

DECIPHER:249519

Abnormality of prenatal development or birth

9625
(4.0%)

MyGene2:2197

Splenomegaly

9625
(4.0%)

DECIPHER:258586

Inguinal hernia

9625
(4.0%)

MyGene2:600

Visual impairment

9625
(4.0%)

MyGene2:163

Hearing impairment

9625
(4.0%)

MyGene2:1963

Dementia

9625
(4.0%)

MyGene2:2140

Autism

9625
(4.0%)

DECIPHER:356372

Hypermetropia

9625
(4.0%)

UDN:069

Bruising susceptibility

9625
(4.0%)

DECIPHER:305118

Dystonia

9625
(4.0%)

DECIPHER:263361

Recurrent urinary tract infections

9625
(4.0%)

MyGene2:1751

Hydronephrosis

9625
(4.0%)

MyGene2:1381

Delayed speech and language development

9625
(4.0%)

DECIPHER:306170

Abnormality iris morphology

9625
(4.0%)

DECIPHER:307556

Abnormality iris morphology

9625
(4.0%)

DECIPHER:303613

Functional abnormality of the bladder

9625
(4.0%)

MyGene2:492

Visual impairment

9625
(4.0%)

DECIPHER:341018

Autistic behavior

9625
(4.0%)

DECIPHER:272251

Strabismus

9625
(4.0%)

DECIPHER:249591

Aplasia of the uterus

9625
(4.0%)

MyGene2:2283

Chronic otitis media

9625
(4.0%)

MyGene2:159

Autism

9625
(4.0%)

UDN:055

Delayed speech and language development

9625
(4.0%)

DECIPHER:285759

Hypermetropia

9625
(4.0%)

MyGene2:482

Strabismus

9625
(4.0%)

DECIPHER:327591

Intellectual disability

9625
(4.0%)

MyGene2:1943

Conductive hearing impairment

9625
(4.0%)

UDN:111

Ptosis

9625
(4.0%)

MyGene2:459

Tall stature

9625
(4.0%)

MyGene2:1639

Seizure

9625
(4.0%)

DECIPHER:351975

Hearing impairment

9625
(4.0%)

MyGene2:214

Aggressive behavior

9625
(4.0%)

MyGene2:1930

Abnormality of eye movement

9625
(4.0%)

MyGene2:2002

Seizure

9625
(4.0%)

UDN:040

Depressivity

9625
(4.0%)

MyGene2:288

Retinal degeneration

9625
(4.0%)

MyGene2:426

Ambiguous genitalia

9625
(4.0%)

MyGene2:347

Anxiety

9625
(4.0%)

MyGene2:1410

Strabismus

9625
(4.0%)

MyGene2:2232

Optic nerve hypoplasia

9625
(4.0%)

MyGene2:1345

Hearing impairment