Severe failure to thrive
Symptom Information:
Symptom ID: | HPO:0001525 | |||||||
Synonyms: |
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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) Growth abnormality(HPO:0001507) Abnormality of body weight(HPO:0004323) Decreased body weight(HPO:0004325) Failure to thrive(HPO:0001508) Severe failure to thrive(HPO:0001525) MedDRA: |
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Database Frequency: | 13 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
COCKAYNE SYNDROME B | (OMIM:133540) |
Cockayne syndrome | (Orphanet:191) |
DIABETES MELLITUS, TRANSIENT NEONATAL, 1 | (OMIM:601410) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |
Leprechaunism | (Orphanet:508) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Osteocraniostenosis | (Orphanet:2763) |
Rhizomelic chondrodysplasia punctata | (Orphanet:177) |
Rhizomelic chondrodysplasia punctata type 1 | (Orphanet:309789) |
Yunis-Varon syndrome | (Orphanet:3472) |