Small for gestational age
Symptom Information:
Symptom ID: | HPO:0001518 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |