Small for gestational age

Symptom Information:

Symptom ID: HPO:0001518
Synonyms:
Birth weight less than 10th percentile [HPO:0001518]
Low birth weight [HPO:0001518]
Low birth weight [OMIM:Low birth weight]
Small for gestational age [OMIM:Small for gestational age]
Low birth weight (2 patients) [OMIM:Low birth weight (2 patients)]
Low birth weight (27%) [OMIM:Low birth weight (27%)]
Low birth weight (some) [OMIM:Low birth weight (some)]
Quality:
Cross references:
OMIM: "Low birth weight" [OMIM:Low birth weight]
OMIM: "Small for gestational age" [OMIM:Small for gestational age]
OMIM: "Low birth weight (2 patients)" [OMIM:Low birth weight (2 patients)]
OMIM: "Low birth weight (27%)" [OMIM:Low birth weight (27%)]
OMIM: "Low birth weight (some)" [OMIM:Low birth weight (some)]
Is a (Direct Parents):
HPO         Decreased body weight
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)
                Small for gestational age(HPO:0001518)
MedDRA:
Database Frequency: 107 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
17p11.2 microduplication syndrome (Orphanet:1713)
17q23.1q23.2 microdeletion syndrome (Orphanet:261279)
1p36 deletion syndrome (Orphanet:1606)
3M syndrome (Orphanet:2616)
3q29 microdeletion syndrome (Orphanet:65286)
5p13 microduplication syndrome (Orphanet:329802)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS (OMIM:201750)
AREDYLD syndrome (Orphanet:1133)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
Apparent mineralocorticoid excess (Orphanet:320)
Autosomal dominant Kenny-Caffey syndrome (Orphanet:93325)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bangstad syndrome (Orphanet:1227)
Bartter syndrome (Orphanet:112)
Bowen-Conradi syndrome (Orphanet:1270)
CATARACT, MICROCEPHALY, FAILURE TO THRIVE, KYPHOSCOLIOSIS SYNDROME (OMIM:212540)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
COCKAYNE SYNDROME B (OMIM:133540)
Cockayne syndrome (Orphanet:191)
Cohen syndrome (Orphanet:193)
Combined oxidative phosphorylation defect type 2 (Orphanet:254920)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
DEND syndrome (Orphanet:79134)
DWARFISM, LEVI TYPE (OMIM:127100)
Developmental malformations - deafness - dystonia (Orphanet:79107)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 15q (Orphanet:1596)
Ear-patella-short stature syndrome (Orphanet:2554)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (OMIM:227650)
FANCONI ANEMIA, COMPLEMENTATION GROUP C (OMIM:227645)
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 (OMIM:227646)
FANCONI ANEMIA, COMPLEMENTATION GROUP E (OMIM:600901)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Familial hyperthyroidism due to mutations in TSH receptor (Orphanet:424)
Fanconi anemia (Orphanet:84)
Fetal akinesia deformation sequence (Orphanet:994)
Fetal akinesia-cerebral and retinal hemorrhage syndrome (Orphanet:363409)
Freeman-Sheldon syndrome (Orphanet:2053)
Galloway-Mowat syndrome (Orphanet:2065)
Hallermann-Streiff syndrome (Orphanet:2108)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
Intestinal epithelial dysplasia (Orphanet:92050)
Isolated glycerol kinase deficiency (Orphanet:408)
Johanson-Blizzard syndrome (Orphanet:2315)
Kenny-Caffey syndrome (Orphanet:2333)
Koolen-De Vries syndrome (Orphanet:96169)
Leprechaunism (Orphanet:508)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
Lowry-Wood syndrome (Orphanet:1824)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, X-LINKED 19 (OMIM:300844)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
Maturity-onset diabetes of the young, type 10 (OMIM:613370)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Microcephalic primordial dwarfism due to ZNF335 deficiency (Orphanet:329228)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency (Orphanet:314637)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Monosomy 18p (Orphanet:1598)
Monosomy 5p (Orphanet:281)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mulibrey nanism (Orphanet:2576)
Neonatal hemochromatosis (Orphanet:446)
Neonatal intrahepatic cholestasis due to citrin deficiency (Orphanet:247598)
OSTEOGENESIS IMPERFECTA, TYPE II (OMIM:166210)
OSTEOGENESIS IMPERFECTA, TYPE XVI (OMIM:616229)
Osteogenesis imperfecta type 2 (Orphanet:216804)
PANCREATIC AGENESIS 2 (OMIM:615935)
Pearson syndrome (Orphanet:699)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
RIENHOFF SYNDROME (OMIM:615582)
Rabson-Mendenhall syndrome (Orphanet:769)
Renal cysts and diabetes syndrome (Orphanet:93111)
Reticular dysgenesis (Orphanet:33355)
SECKEL SYNDROME 2 (OMIM:606744)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
SHORT syndrome (Orphanet:3163)
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 (OMIM:604320)
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE (OMIM:613320)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Shwachman-Diamond syndrome (Orphanet:811)
Silver-Russell syndrome (Orphanet:813)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Syndromic diarrhea (Orphanet:84064)
TEMPLE SYNDROME (OMIM:616222)
THREE M SYNDROME 1 (OMIM:273750)
THREE M SYNDROME 3 (OMIM:614205)
THYROID HORMONE RESISTANCE, GENERALIZED, AUTOSOMAL RECESSIVE (OMIM:274300)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked immunoneurologic disorder (Orphanet:2571)
Xq27.3q28 duplication syndrome (Orphanet:261483)