Postnatal growth retardation
Symptom Information:
Symptom ID: | HPO:0008897 | ||||||||||||||||
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) Growth delay(HPO:0001510) Postnatal growth retardation(HPO:0008897) MedDRA: |
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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) |