Failure to thrive in infancy

Symptom Information:

Symptom ID: HPO:0001531
Synonyms:
Failure to thrive in first year of life [HPO:0001531]
Failure to thrive in first year of life [OMIM:Failure to thrive in first year of life]
Failure to thrive in infancy [OMIM:Failure to thrive in infancy]
Quality:
Cross references:
OMIM: "Failure to thrive in first year of life" [OMIM:Failure to thrive in first year of life]
OMIM: "Failure to thrive in infancy" [OMIM:Failure to thrive in infancy]
Is a (Direct Parents):
HPO         Failure to thrive
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:
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)