Postnatal growth retardation

Symptom Information:

Symptom ID: HPO:0008897
Synonyms:
Growth retardation as children [HPO:0008897]
Postnatal growth deceleration [HPO:0008897]
Postnatal growth deficiency [HPO:0008897]
Postnatal growth failure [HPO:0008897]
Growth retardation as children [OMIM:Growth retardation as children]
Postnatal growth deceleration [OMIM:Postnatal growth deceleration]
Postnatal growth deficiency [OMIM:Postnatal growth deficiency]
Postnatal growth failure [OMIM:Postnatal growth failure]
Postnatal growth retardation [OMIM:Postnatal growth retardation]
Growth failure, postnatal [OMIM:Growth failure, postnatal]
Growth retardation, postnatal [OMIM:Growth retardation, postnatal]
Postnatal growth deficiency (50%) [OMIM:Postnatal growth deficiency (50%)]
Postnatal growth retardation (-7 S.D.) [OMIM:Postnatal growth retardation (-7 S.D.)]
Postnatal growth retardation (deletion patients) [OMIM:Postnatal growth retardation (deletion patients)]
Postnatal growth retardation (in some patients) [OMIM:Postnatal growth retardation (in some patients)]
Postnatal growth retardation (some patients) [OMIM:Postnatal growth retardation (some patients)]
Quality:
Cross references:
OMIM: "Growth retardation as children" [OMIM:Growth retardation as children]
OMIM: "Postnatal growth deceleration" [OMIM:Postnatal growth deceleration]
OMIM: "Postnatal growth deficiency" [OMIM:Postnatal growth deficiency]
OMIM: "Postnatal growth failure" [OMIM:Postnatal growth failure]
OMIM: "Postnatal growth retardation" [OMIM:Postnatal growth retardation]
OMIM: "Growth failure, postnatal" [OMIM:Growth failure, postnatal]
OMIM: "Growth retardation, postnatal" [OMIM:Growth retardation, postnatal]
OMIM: "Postnatal growth deficiency (50%)" [OMIM:Postnatal growth deficiency (50%)]
OMIM: "Postnatal growth retardation (-7 S.D.)" [OMIM:Postnatal growth retardation (-7 S.D.)]
OMIM: "Postnatal growth retardation (deletion patients)" [OMIM:Postnatal growth retardation (deletion patients)]
OMIM: "Postnatal growth retardation (in some patients)" [OMIM:Postnatal growth retardation (in some patients)]
OMIM: "Postnatal growth retardation (some patients)" [OMIM:Postnatal growth retardation (some patients)]
Is a (Direct Parents):
HPO         Growth delay
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)
MedDRA:
Database Frequency: 113 / 7739
Resource:

All diseases associated with this symptom:

17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
19q13.11 microdeletion syndrome (Orphanet:217346)
2q23.1 microdeletion syndrome (Orphanet:228402)
3-phosphoserine phosphatase deficiency (Orphanet:79350)
3M syndrome (Orphanet:2616)
3MC SYNDROME 1 (OMIM:257920)
3MC SYNDROME 2 (OMIM:265050)
3MC SYNDROME 3 (OMIM:248340)
4q21 microdeletion syndrome (Orphanet:238750)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
Acrocallosal syndrome (Orphanet:36)
Aicardi syndrome (Orphanet:50)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Anophthalmia/microphthalmia - esophageal atresia (Orphanet:77298)
Argininemia (Orphanet:90)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Baraitser-Winter syndrome (Orphanet:2995)
Bloom syndrome (Orphanet:125)
Branchio-oculo-facial syndrome (Orphanet:1297)
CATEL-MANZKE SYNDROME (OMIM:616145)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
COCKAYNE SYNDROME B (OMIM:133540)
COFFIN-SIRIS SYNDROME (OMIM:135900)
COG1-CDG (Orphanet:263508)
COLE-CARPENTER SYNDROME 2 (OMIM:616294)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Catel-Manzke syndrome (Orphanet:1388)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Coats plus syndrome (Orphanet:313838)
Cockayne syndrome (Orphanet:191)
Coffin-Siris syndrome (Orphanet:1465)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
DYGGVE-MELCHIOR-CLAUSEN DISEASE (OMIM:223800)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 (OMIM:615190)
Dilated cardiomyopathy with ataxia (Orphanet:66634)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 3p (Orphanet:1620)
Distal renal tubular acidosis (Orphanet:18)
Dubowitz syndrome (Orphanet:235)
Dyggve-Melchior-Clausen disease (Orphanet:239)
Ehlers-Danlos syndrome, spondylocheirodysplastic type (Orphanet:157965)
FANCONI ANEMIA, COMPLEMENTATION GROUP J (OMIM:609054)
FANCONI ANEMIA, COMPLEMENTATION GROUP N (OMIM:610832)
Filippi syndrome (Orphanet:3255)
Freeman-Sheldon syndrome (Orphanet:2053)
GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGEJOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLARATROPHY (OMIM:608278)
GROWTH HORMONE DEFICIENCY, ISOLATED PARTIAL (OMIM:615925)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glycogen storage disease due to liver glycogen phosphorylase deficiency (Orphanet:369)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 (OMIM:615361)
Hypotonia-speech impairment-severe cognitive delay syndrome (Orphanet:371364)
IMAGe syndrome (Orphanet:85173)
INTRAUTERINE GROWTH RETARDATION WITH INCREASED MITOMYCIN C SENSITIVITY (OMIM:600546)
Immunodeficiency with natural-killer cell deficiency (Orphanet:75391)
Intellectual deficit, X-linked, Wilson type (Orphanet:85290)
Joubert syndrome 5 (OMIM:610188)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
Leprechaunism (Orphanet:508)
Lissencephaly type 1 due to doublecortin gene mutation (Orphanet:2148)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MGAT2-CDG (Orphanet:79329)
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE (OMIM:612947)
MOVED TO 614732 (OMIM:300290)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Marden-Walker syndrome (Orphanet:2461)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microphthalmia with limb anomalies (Orphanet:1106)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Mitochondrial myopathy - lactic acidosis - deafness (Orphanet:2597)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mulibrey nanism (Orphanet:2576)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
POLYENDOCRINE-POLYNEUROPATHY SYNDROME (OMIM:616113)
Peters-plus syndrome (Orphanet:709)
Postaxial acrofacial dysostosis (Orphanet:246)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Rabson-Mendenhall syndrome (Orphanet:769)
Recombinant 8 syndrome (Orphanet:96167)
Renal cysts and diabetes syndrome (Orphanet:93111)
Roberts syndrome (Orphanet:3103)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SECKEL SYNDROME 1 (OMIM:210600)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Sanjad-Sakati syndrome (Orphanet:2323)
Schinzel-Giedion syndrome (Orphanet:798)
Senior-Loken syndrome 6 (OMIM:610189)
Senior-Loken syndrome 8 (OMIM:616307)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondylometaphyseal dysplasia - cone-rod dystrophy (Orphanet:85167)
THREE M SYNDROME 1 (OMIM:273750)
VACTERL/VATER association (Orphanet:887)
WARBURG MICRO SYNDROME 2 (OMIM:614225)
WARBURG MICRO SYNDROME 3 (OMIM:614222)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked intellectual deficit, Najm type (Orphanet:163937)