All diseases

OMIM ID
210710
OMIM term:
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1
Alternative terms:
MOPD I; MOPD
OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
BRACHYMELIC PRIMORDIAL DWARFISM
TAYBI-LINDER SYNDROME; TALS
CEPHALOSKELETAL DYSPLASIA
LOW-BIRTH-WEIGHT DWARFISM WITH SKELETAL DYSPLASIA
(∗) Location:
2q14.2  
(†) Associated OMIM genes:
RNU4ATAC  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/decucqsu