Failure to thrive in infancy
Symptom Information:
Symptom ID: | HPO:0001531 | |||
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) Failure to thrive in infancy(HPO:0001531) MedDRA: |
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Database Frequency: | 26 / 7739 | |||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
CEREBROOCULOFACIOSKELETAL SYNDROME 4 | (OMIM:610758) |
COG1-CDG | (Orphanet:263508) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Costello syndrome | (Orphanet:3071) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Hypotonia - failure to thrive - microcephaly | (Orphanet:79507) |
Isolated sedoheptulokinase deficiency | (ORPHA:440713) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 7 | (OMIM:614104) |
Monosomy 18q | (Orphanet:1600) |
Multiple endocrine neoplasia type 2B | (Orphanet:247709) |
NOONAN SYNDROME 1 | (OMIM:163950) |
Neonatal diabetes mellitus | (Orphanet:224) |
Neonatal hemochromatosis | (Orphanet:446) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Prader-Willi syndrome | (Orphanet:739) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |
Transaldolase deficiency | (Orphanet:101028) |
Transient neonatal diabetes mellitus | (Orphanet:99886) |
Williams syndrome | (Orphanet:904) |
X-linked reticulate pigmentary disorder with systemic manifestations | (Orphanet:85453) |