|
41
|
|
|
Developing brain homeobox 1 |
HLX1 |
|
|
42
|
|
|
DnaJ heat shock protein family (Hsp40) member C24 |
DPH4, JJJ3, ZCSL3 |
|
|
43
|
|
|
Dynein axonemal assembly factor 1 |
CILD13, DAU1, LRRC50, ODA7, swt |
Asthenozoospermia, Asthma, Bronchiectasis, Bronchitis, Ciliary dyskinesia, Ciliopathies, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Hearing loss, Hydrocephalus, Hypertension, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (4 more) |
|
44
|
|
|
Defective in cullin neddylation 1 domain containing 3 |
44M2.4, DCNL3, SCCRO3 |
|
|
45
|
|
|
Diencephalon/mesencephalon homeobox 1 |
Atx, MBX, OTX3, PAXB |
|
|
46
|
|
|
DNA damage regulated autophagy modulator 2 |
CORD21, PRO180, TMEM77, WWFQ154 |
|
|
47
|
|
|
DIS3 like 3'-5' exoribonuclease 2 |
FAM6A, PRLMNS, hDIS3L2 |
Agenesis of corpus callosum, Aniridia, Cardiovascular abnormalities, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Dolichocephaly, Hernia, femoral, Hyperinsulinism, Hypertension, Interrupted aortic arch, Intestinal volvulus, Liver neoplasms, Lung neoplasms, Macrocephaly, Mental retardation, Micrognathism, Nephroblastoma, Perlman syndrome, Posteriorly rotated ear, Ptosis, Specific learning disorder, Status epilepticus, Strawberry nevus of skinView all (11 more) |
|
48
|
|
|
DnaJ heat shock protein family (Hsp40) member C19 |
PAM18, TIM14, TIMM14 |
3-methylglutaconic aciduria, Amyotrophy, Anemia, Arachnoid cyst, Brainstem atrophy, Cardiomyopathy, Congenital hypoplasia of penis, Congestive heart failure, Cryptorchidism, Developmental delay, Developmental regression, Diaphragmatic eventration, Dilated cardiomyopathy with ataxia, Dyskinetic syndrome, Hypospadias, Hypothyroidism, Mental retardation, Microcytic anemia, Muscular ventricular septal defect, Hypoglycemia, Hypotonia, Noncompaction cardiomyopathy, Optic atrophy, Repetitive compulsive behavior, Sensorineural hearing lossView all (10 more) |
|
49
|
|
|
Discoidin, CUB and LCCL domain containing 2 |
CLCP1, ESDN |
|
|
50
|
|
|
DnaJ heat shock protein family (Hsp40) member C21 |
BMFS3, DNAJA5, GS3, JJJ1 |
Amelogenesis imperfecta, Anemia, Aphthous ulcer, Aplastic anemia, Astigmatism, Bone marrow failure syndrome, Breast cancer, Congenital alveolar dysplasia, Developmental dysplasia of the hip, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Cryptorchidism, Dental enamel hypoplasia, Developmental delay, Diabetes mellitus, Dwarfism, Eczema, Exocrine pancreatic insufficiency, Hyperkeratosis, Hyperopia, Ichthyosis, Impaired cognition, Inherited bone marrow failure syndrome, Leukemia, Malabsorption syndrome, Mental retardation, Metaphyseal chondrodysplasia, Microdontia, Micrognathism, Myelodysplasia, Myelodysplastic syndrome, Myocardial infarction, Myocardial necrosis, Myopia, Nail dystrophy, Neck webbing, Nephrocalcinosis, Neutropenia, Osteopenia, Pancytopenia, Scoliosis, Shwachman syndrome, Shwachman-diamond syndrome, Slipped capital femoral epiphyses, Specific learning disorderView all (31 more) |
