Severe postnatal growth retardation

Symptom Information:

Symptom ID: HPO:0008850
Synonyms:
Marked growth retardation [HPO:0008850]
Severe postnatal growth deficiency [HPO:0008850]
Severe postnatal growth failure [HPO:0008850]
Marked growth retardation [OMIM:Marked growth retardation]
Severe postnatal growth deficiency [OMIM:Severe postnatal growth deficiency]
Marked growth retardation (-3 S.D.) [OMIM:Marked growth retardation (-3 S.D.)]
Postnatal growth retardation, severe [OMIM:Postnatal growth retardation, severe]
Quality:
Cross references:
OMIM: "Marked growth retardation" [OMIM:Marked growth retardation]
OMIM: "Severe postnatal growth deficiency" [OMIM:Severe postnatal growth deficiency]
OMIM: "Marked growth retardation (-3 S.D.)" [OMIM:Marked growth retardation (-3 S.D.)]
OMIM: "Postnatal growth retardation, severe" [OMIM:Postnatal growth retardation, severe]
Is a (Direct Parents):
HPO         Postnatal growth retardation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Postnatal growth retardation(HPO:0008897)
                Severe postnatal growth retardation(HPO:0008850)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

4q21 microdeletion syndrome (Orphanet:238750)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
BAINBRIDGE-ROPERS SYNDROME (OMIM:615485)
COCKAYNE SYNDROME A (OMIM:216400)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
Isolated thyroid-stimulating hormone deficiency (Orphanet:90674)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Mietens syndrome (Orphanet:2557)
Mucolipidosis type 2 (Orphanet:576)
PITUITARY HORMONE DEFICIENCY, COMBINED, 1 (OMIM:613038)
Parana hard-skin syndrome (Orphanet:2812)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
RENAL AND MULLERIAN DUCT HYPOPLASIA (OMIM:266810)
Short stature - pituitary and cerebellar defects - small sella turcica (Orphanet:85442)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
Wolf-Hirschhorn syndrome (Orphanet:280)