|
1991
|
|
|
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) |
|
1992
|
|
|
Transmembrane protein 171 |
PRP2 |
|
|
1993
|
|
|
POC5 centriolar protein |
C5orf37 |
|
|
1994
|
|
|
WD repeat domain 36 |
GLC1G, TA-WDRP, TAWDRP, UTP21 |
|
|
1995
|
|
|
Zinc finger protein 300 pseudogene 1 |
- |
|
|
1996
|
|
|
Cytochrome c oxidase subunit 6C |
- |
|
|
1997
|
|
|
Ubiquitin like domain containing CTD phosphatase 1 |
CPUB1 |
|
|
1998
|
|
|
Ripply transcriptional repressor 2 |
C6orf159, SCDO6, dJ237I15.1 |
Abnormal spinal segmentation, Congenital diaphragmatic hernia, Congenital exomphalos, Rib fusion, Congenital meningocele, Cryptorchidism, Dextrocardia, Dwarfism, Hypospadias, Jarcho-levin syndrome, Klippel feil syndrome, Macrocephaly, Mental retardation, Microcephaly, Pulmonary venous return anomaly, Scoliosis, Spina bifida occulta, Spondylocostal dysostosis, Syndactyly of fingersView all (4 more) |
|
1999
|
|
|
Interleukin 1 receptor associated kinase 1 binding protein 1 |
AIP70, SIMPL |
Attention deficit hyperactivity disorder, Autism, Behavioral abnormality, Developmental delay, intellectual disability, obesity, and dysmorphic features, Mental retardation, Hypotonia, Obsessive-compulsive disorder, Sjogren`s syndrome |
|
2000
|
|
|
Clavesin 2 |
C6orf212, C6orf213, RLBP1L2, bA160A10.4 |
|
