Mild short stature
Symptom Information:
Symptom ID: | HPO:0003502 | |||||||
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 height(HPO:0000002) Short stature(HPO:0004322) Proportionate short stature(HPO:0003508) Mild short stature(HPO:0003502) Growth delay(HPO:0001510) Short stature(HPO:0004322) Proportionate short stature(HPO:0003508) Mild short stature(HPO:0003502) MedDRA: |
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Database Frequency: | 19 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
AARSKOG-SCOTT SYNDROME | (OMIM:305400) |
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:614613) |
Aarskog-Scott syndrome | (Orphanet:915) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
BARATELA-SCOTT SYNDROME | (OMIM:300881) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
DIGITOTALAR DYSMORPHISM | (OMIM:126050) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 2 | (OMIM:600204) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 3 | (OMIM:600969) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Metaphyseal chondrodysplasia, Schmid type | (Orphanet:174) |
Mononen-Karnes-Senac syndrome | (Orphanet:2565) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple epiphyseal dysplasia due to collagen 9 anomaly | (Orphanet:166002) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
PELGER-HUET ANOMALY | (OMIM:169400) |
STIFF SKIN SYNDROME | (OMIM:184900) |
WIDOW'S PEAK SYNDROME | (OMIM:314570) |