|
3431
|
|
|
TBC1 domain family member 2B |
NEDSGO |
|
|
3432
|
|
|
Follistatin like 4 |
- |
|
|
3433
|
|
|
Mitochondrial ribosomal protein S27 |
MRP-S27, S27mt, mS27 |
|
|
3434
|
|
|
Dendrin |
- |
|
|
3435
|
|
|
Spartin |
SPG20, TAHCCP1 |
Acquired kyphoscoliosis, Anxiety disorder, Apraxia, Brachydactyly, Cerebellar atrophy, Clinodactyly, Congenital camptodactyly, Congenital epicanthus, Congenital kyphoscoliosis, Developmental delay, Distal amyotrophy, Dwarfism, Dysarthria, Dysmorphic features, Dysphagia, Dyssomnia, Esophageal cancer, Hallucinations, Hydronephrosis, Impaired cognition, Mental retardation, Microcephaly, Mood swings, Motor delay, Panic disorder, Psychosis, Sleep disorders, Spastic paraplegia, Specific learning disorder, Strabismus, Troyer syndromeView all (16 more) |
|
3436
|
|
|
Trinucleotide repeat containing adaptor 6B |
GDSBA |
|
|
3437
|
|
|
Cullin 9 |
H7AP1, PARC |
|
|
3438
|
|
|
Neurofascin |
NEDCPMD, NF, NRCAML |
|
|
3439
|
|
|
TGF-beta activated kinase 1 (MAP3K7) binding protein 2 |
CHTD2, MAP3K7IP2, TAB-2 |
6q24-q25 deletion syndrome, Aortic aneurysm, Aortic valve insufficiency, Aortic valve sclerosis, Atrial fibrillation, Bicuspid aortic valve, Breast cancer, Breast carcinoma, Congenital heart defects, Crohn disease, Diabetes mellitus, Dolichocephaly, Dwarfism, High palate, Inflammatory bowel disease, Mental retardation, Micrognathism, Mitral valve dysplasia, Mitral valve prolapse, Polyvalvular heart disease syndrome, Ptosis, Pulmonary stenosis, Rectal prolapse, Secundum atrial septal defect, Subaortic stenosis, Tetralogy of fallot, Tricuspid valve insufficiency, Ventricular septal defectView all (13 more) |
|
3440
|
|
|
Filaggrin |
ATOD2, FLG-1, FLG1 |
Asthma, Autism, Cerebellar hypoplasia, Cutis marmorata, Dermatitis, Developmental delay, Dysmorphic features, Eczema, Hypospadias, Ichthyosis, Ichthyosis vulgaris, Movement disorders, Myopia, Nystagmus, Osteopenia, Respiratory tract diseasesView all (1 more) |
