Developmental stagnation
Symptom Information:
Symptom ID: | HPO:0007281 | ||
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) Developmental regression(HPO:0002376) Developmental stagnation(HPO:0007281) MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Adenylosuccinate lyase deficiency | (Orphanet:46) |
CEREBROCORTICAL DEGENERATION OF INFANCY | (OMIM:213950) |
GM1 gangliosidosis type 2 | (Orphanet:79256) |
Mucolipidosis type 4 | (Orphanet:578) |
PEHO syndrome | (Orphanet:2836) |
STRIATONIGRAL DEGENERATION, INFANTILE | (OMIM:271930) |