|
261
|
|
|
Delta like canonical Notch ligand 1 |
DELTA1, DL1, Delta, NEDBAS |
Agenesis of corpus callosum, Alobar holoprosencephaly, Ambiguous genitalia, Asthma, Autism, Brain neoplasms, Breast cancer, Mammary neoplasms, Breast carcinoma, Intracranial neoplasm, Choanal atresia, Congenital coloboma of iris, Congenital hypoplasia of penis, Cyclocephaly, Developmental delay, Duodenal atresia, Dwarfism, Fused incisors, Hemangioma, Holoprosencephaly, Hypothyroidism, Lobar holoprosencephaly, Marfan syndrome, Mental retardation, Microcephaly, Microform holoprosencephaly, Midline interhemispheric variant of holoprosencephaly, Panhypopituitarism, Renal agenesis, Scoliosis, Semilobar holoprosencephaly, Septopreoptic holoprosencephaly, Strabismus, Tetralogy of fallotView all (19 more) |
|
262
|
|
|
Docking protein 7 |
C4orf25, CMS10, CMS1B, FADS3 |
Akinesia, Amyotrophy, Arthrogryposis multiplex congenita, Bulbar palsy, Pulmonary hypoplasia, Myasthenic syndrome, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Distal amyotrophy, Facial paralysis, Fetal akinesia deformation sequence, High palate, Limb-girdle muscular dystrophy, Cystic hygroma, Micrognathism, Muscular dystrophy, Myasthenia gravis, Pena shokeir syndrome, Posteriorly rotated ear, Pterygium, Ptosis, Respiratory failure, ScoliosisView all (9 more) |
|
263
|
|
|
Discoidin, CUB and LCCL domain containing 1 |
dJ94G16.1 |
|
|
264
|
|
|
Decapping enzyme, scavenger |
ARS, DCS1, HINT-5, HINT5, HSL1, HSPC015 |
Absence of septum pellucidum, Al-raqad syndrome, Autism, Brachydactyly, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypopigmentation disorder, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Microstomia, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (8 more) |
|
265
|
|
|
Drebrin like |
ABP1, HIP-55, HIP55, SH3P7 |
|
|
266
|
|
|
Drosha ribonuclease III |
ETOHI2, HSA242976, RANSE3L, RN3, RNASE3L, RNASEN |
|
|
267
|
|
|
DnaJ heat shock protein family (Hsp40) member C15 |
DNAJD1, HSD18, MCJ |
|
|
268
|
|
|
DEAD-box helicase 25 |
GRTH |
|
|
269
|
|
|
Dermatan sulfate epimerase |
DS-epi1, DSEP, DSEPI, EDSMC2, SART-2, SART2 |
Arachnodactyly, Brachycephaly, Cerebral atrophy, Congenital camptodactyly, Congenital clubfoot, Developmental delay, Musculocontractural ehlers-danlos syndrome, Frontal bossing, High palate, Microstomia, Mitral valve prolapse, Patent foramen ovale |
|
270
|
|
|
DNA methyltransferase 3 like |
- |
|
