|
mental retardation, autosomal recessive 49
|
14567 |
|
|
mental retardation, autosomal recessive 49; MRT49
|
http://purl.obolibrary.org/obo/MONDO_0014567 |
|
|
mental retardation, autosomal recessive type 49
|
14567 |
|
|
postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome
|
14567 |
|
|
type 2 simpson-golabi-behmel syndrome
|
C564567 |
|
|
NALCN hypotonia, infantile, with psychomotor retardation and characteristic facies
|
24567 |
|
|
glutamate pyruvate transaminase 2 deficiency
|
14567 |
|
|
hypotonia, infantile, with psychomotor retardation and characteristic facies 1
|
24567 |
|
|
hypotonia, infantile, with psychomotor retardation and characteristic facies 1; IHPRF1
|
http://purl.obolibrary.org/obo/MONDO_0024567 |
|
