Mild global developmental delay

Symptom Information:

Symptom ID: HPO:0011342
Synonyms:
Global developmental delay, mild [OMIM:Global developmental delay, mild]
Quality:
Cross references:
OMIM: "Global developmental delay, mild" [OMIM:Global developmental delay, mild]
Is a (Direct Parents):
HPO         Global developmental delay
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system physiology(HPO:0012638)
             Abnormality of higher mental function(HPO:0011446)
                Cognitive impairment(HPO:0100543)
                   Global developmental delay(HPO:0001263)
                      Mild global developmental delay(HPO:0011342)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Isobutyryl-CoA dehydrogenase deficiency (Orphanet:79159)
Maternally-inherited cardiomyopathy and hearing loss (Orphanet:1349)
Mucopolysaccharidosis type 2 (Orphanet:580)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
RIDDLE SYNDROME (OMIM:611943)
Rabson-Mendenhall syndrome (Orphanet:769)
SECKEL SYNDROME 2 (OMIM:606744)