|
661
|
|
|
Methyltransferase 9, His-X-His N1(pi)-histidine |
CGI-81, DREV, DREV1, PAP1, hMETTL9 |
|
|
662
|
|
|
Mitochondrial ribosomal protein S2 |
CGI-91, COXPD36, MRP-S2, S2mt, uS2m |
|
|
663
|
|
|
MRN complex interacting protein |
C5orf45 |
|
|
664
|
|
|
Myosin XVA |
DFNB3, MYO15 |
|
|
665
|
|
|
Mitochondrial ribosomal protein L37 |
L2mt, L37mt, MRP-L2, MRP-L37, MRPL2, RPML2, mL37 |
|
|
666
|
|
|
Mex-3 RNA binding family member C |
BM-013, MEX-3C, RKHD2, RNF194 |
|
|
667
|
|
|
Membrane spanning 4-domains A4A |
4SPAN1, CD20-L1, CD20L1, HDCME31P, MS4A4, MS4A7 |
|
|
668
|
|
|
Membrane bound transcription factor peptidase, site 2 |
BRESEK, IFAP, KFSD, KFSDX, OI19, OLMSX, S2P |
Absence of septum pellucidum, Absent eyebrow, Agenesis of corpus callosum, Alopecia, Anhidrosis, Astigmatism, Brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear-eye anomalies, cleft palate-cryptorchidism, and kidney dysplasia-hypoplasia, Brain atrophy, Bresek syndrome, Cerebellar hypoplasia, Cerebral atrophy, Cerebral cortical hemiatrophy, Cheilitis, Choanal atresia, Congenital coloboma of iris, Congenital exomphalos, Congenital omphalocele, Congenital pectus carinatum, Congenital pectus excavatum, Conjunctivitis, Corneal dystrophy, Corneal erosion, Cryptorchidism, Dementia, Developmental delay, Developmental regression, Dwarfism, Ectodermal dysplasia, Ectrodactyly, Ectropion, Eczema, Episcleritis, Erosion of cornea, Exfoliative dermatitis, Folliculitis, Frontal bossing, Hearing loss, Hirschsprung disease, Hydrocephalus, Hydronephrosis, Hyperhidrosis palmaris et plantaris, Hyperkeratosis, Hypodontia, Hypohidrosis, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Hypotrichosis, Ichthyosis, Ichthyosis follicularis atrichia photophobia syndrome, Ichthyosis follicularis-alopecia-photophobia syndrome, Immunologic deficiency syndromes, Mental retardation, Keratitis, Keratosis follicularis spinulosa decalvans, Keratosis follicularis spinulosa decalvans, x-linked, Keratosis pilaris, Liver carcinoma, Lung neoplasms, Macrotia, Meibomian gland dysfunction, Melanoma, Microcephaly, Microphthalmos, Multicystic renal dysplasia, Mutilating palmoplantar keratoderma with periorificial keratotic plaques, Myopia, Nail diseases, Nail dysplasia, Nail dystrophy, Nystagmus, Oligodactyly, Olivopontocerebellar atrophies, Olmsted syndrome, Osteogenesis imperfecta, Osteopenia, Palmoplantar keratoderma, Palmoplantar keratoderma, with periorificial keratotic plaques, x-linked, Palmoplantar keratosis, Parakeratosis, Phrynoderma, Plagiocephaly, Polydactyly, Pseudopelade, Renal aplasia, Renal dysplasia, Renal hypoplasia, Rhizomelia, Scleritis, Scoliosis, Skin neoplasms, Specific learning disorder, Subcortical cerebral atrophy, Subungual hyperkeratosis, Postaxial hand polydactyly, Urticaria, Uveitis, Vesicoureteral refluxView all (82 more) |
|
669
|
|
|
MAGE family member C2 |
CT10, HCA587, MAGEE1 |
|
|
670
|
|
|
Mediator complex subunit 15 |
ARC105, CAG7A, CTG7A, PCQAP, TIG-1, TIG1, TNRC7 |
|
