All diseases

OMIM ID
210600
OMIM term:
SECKEL SYNDROME 1; SCKL1
Alternative terms:
SCKL
SECKEL-TYPE DWARFISM
NANOCEPHALIC DWARFISM
MICROCEPHALIC PRIMORDIAL DWARFISM I
BIRD-HEADED DWARFISM
(∗) Location:
3q23  
(†) Associated OMIM genes:
ATR  
(‡) Associated MGI genes:
Atr  

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* quick link - http://q.sanger.ac.uk/6els3dv1