TMEM11 - transmembrane protein 11 Gene

Complex Cortical Dysplasia With Other Brain Malformations 3

CDCBM3

Dysplasia ,Cortical, Complex, With Other Brain Malformations, Type 3

DCUA

DFNA69

Deafness, Congenital, Unilateral Or Asymmetric

Deafness, Autosomal Dominant 69, Unilateral Or Asymmetric

Autosomal Dominant Nonsyndromic Deafness 69

Autosomal Dominant Deafness 69

Unilateral Or Asymmetric Congenital Deafness

COXPD21

Combined Oxidative Phosphorylation Defect Type 21

Combined Oxidative Phosphorylation Deficiency, Type 21

Autosomal Dominant Non-Syndromic Intellectual Disability 31

Autosomal Dominant Mental Retardation 31

Mrd31

X-Linked Epilepsy-Learning Disabilities-Behavior Disorders Syndrome

EPILX

X-Linked Epilepsy With Variable Learning Disabilities And Behavior Disorders

Epilepsy, X-Linked, With Reflex Bathing Seizures

Bathing Epilepsy, X-Linked

PARK17

Parkinson'S Disease 17

Autosomal Dominant Parkinson Disease 17

Parkinson Disease, Type 17

Trichorhinophalangeal Syndrome Type Iii

TRPS3

Sugio-Kajii Syndrome

Trichorhinophalangeal Syndrome Type 3

Trps 3

Tricho-Rhino-Phalangeal Syndrome 3

Adenoid Cystic Carcinoma Of Parotid Gland

Isolated Hyperchlorhidrosis

HYCHL

Carbonic Anhydrase Xii Deficiency

Pediculosis Capitis

Pediculus Capitis Infestation

Head Louse Infestation

Pediculus Capitis

Head-Louse Infestation

Head Lice

Infestation By Pediculus Capitis

Arc Syndrome

ARCS1

Arthrogryposis Renal Dysfunction Cholestasis Syndrome

Arthrogryposis-Renal Dysfunction-Cholestasis Syndrome

Arcs

Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome

Arthrogryposis, Renal Dysfunction, And Cholestasis

Arthrogryposis-Renal Dysfunction-Cholestasis

Arthrogryposis - Renal Dysfunction - Cholestasis

Arthrogryposis Multiplex Congenita, Renal Dysfunction, And Cholestasis

Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome 1

Arthrogryposis Renal Dysfunction And Cholestasis 1

Arthrogryposis With Renal Dysfunction And Cholestasis Syndrome

Arthrogryposis, Renal Dysfunction, Cholestasis, Type 1

Kidney Failure

Renal Insufficiency

FSGS1

Glomerulosclerosis, Focal Segmental, 1

Glomerulosclerosis, Segmental, Focal, Type 1

Segmental Glomerulosclerosis

X-Linked Colobomatous Microphthalmia-Microcephaly-Intellectual Disability-Short Stature Syndrome

MCOPS13

Maine Microphthalmos

Colobomatous Microphthalmia With Microcephaly, Short Stature, And Psychomotor Retardation

Syndromic Microphthalmia 13

X-Linked Colobomatous Microphthalmia-Microcephaly-Short Stature-Psychomotor Retardation Syndrome

Microphthalmia, Syndromic, 13

Microphthalmia, Syndromic, Type 13

Body Louse Infestation

Pediculus Corporis

Pediculus Humanus Infestation

DEE87

Epileptic Encephalopathy, Early Infantile, 87

Eiee87

Developmental And Epileptic Encephalopathy, 87

Early Infantile Epileptic Encephalopathy 87

Malignant Neoplasm Of Hard Palate

Malignant Tumor Of Hard Palate

Malignant Tumour Of Hard Palate

Kallmann Syndrome 2

Kal2

HH2

Hypogonadism, Hypogonadotropic, Type 2 With/Without Anosmia

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant