Mild short stature

Symptom Information:

Symptom ID: HPO:0003502
Synonyms:
Relative short stature [HPO:0003502]
short stature, mild [HPO:0003502]
Relative short stature [OMIM:Relative short stature]
Short stature, mild [OMIM:Short stature, mild]
Relative short stature (compared to unaffected males in family) [OMIM:Relative short stature (compared to unaffected males in family)]
Short stature, mild (in some) [OMIM:Short stature, mild (in some)]
Short stature, relative (in some patients) [OMIM:Short stature, relative (in some patients)]
Quality:
Cross references:
OMIM: "Relative short stature" [OMIM:Relative short stature]
OMIM: "Short stature, mild" [OMIM:Short stature, mild]
OMIM: "Relative short stature (compared to unaffected males in family)" [OMIM:Relative short stature (compared to unaffected males in family)]
OMIM: "Short stature, mild (in some)" [OMIM:Short stature, mild (in some)]
OMIM: "Short stature, relative (in some patients)" [OMIM:Short stature, relative (in some patients)]
Is a (Direct Parents):
HPO         Proportionate short stature
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Growth abnormality(HPO:0001507)
          Growth delay(HPO:0001510)
             Short stature(HPO:0004322)
                Proportionate short stature(HPO:0003508)
                   Mild short stature(HPO:0003502)
          Abnormality of body height(HPO:0000002)
             Short stature(HPO:0004322)
                Proportionate short stature(HPO:0003508)
                   Mild short stature(HPO:0003502)
MedDRA:
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)