Mild global developmental delay
Symptom Information:
Symptom ID: | HPO:0011342 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |