Severe failure to thrive

Symptom Information:

Symptom ID: HPO:0001525
Synonyms:
Marked failure to thrive [HPO:0001525]
Severe postnatal failure to thrive [HPO:0001525]
Marked failure to thrive [OMIM:Marked failure to thrive]
Severe failure to thrive [OMIM:Severe failure to thrive]
Severe postnatal failure to thrive [OMIM:Severe postnatal failure to thrive]
Failure to thrive, severe [OMIM:Failure to thrive, severe]
Failure to thrive, severe (2p21del) [OMIM:Failure to thrive, severe (2p21del)]
Quality:
Cross references:
OMIM: "Marked failure to thrive" [OMIM:Marked failure to thrive]
OMIM: "Severe failure to thrive" [OMIM:Severe failure to thrive]
OMIM: "Severe postnatal failure to thrive" [OMIM:Severe postnatal failure to thrive]
OMIM: "Failure to thrive, severe" [OMIM:Failure to thrive, severe]
OMIM: "Failure to thrive, severe (2p21del)" [OMIM:Failure to thrive, severe (2p21del)]
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)
                   Severe failure to thrive(HPO:0001525)
MedDRA:
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)