Neonatal epiphyseal stippling

Symptom Information:

Symptom ID: HPO:0005756
Synonyms:
Epiphyseal stippling in neonates [HPO:0005756]
Epiphyseal stippling in neonates (lumbosacral and cervical bodies, carpus, tarsus, proximal humerus, terminal phalanges, knees, hips) [OMIM:Epiphyseal stippling in neonates (lumbosacral and cervical bodies, carpus, tarsus, proximal humerus, terminal phalanges, knees, hips)]
Quality:
Cross references:
OMIM: "Epiphyseal stippling in neonates (lumbosacral and cervical bodies, carpus, tarsus, proximal humerus, terminal phalanges, knees, hips)" [OMIM:Epiphyseal stippling in neonates (lumbosacral and cervical bodies, carpus, tarsus, proximal humerus, terminal phalanges, knees, hips)]
Is a (Direct Parents):
HPO         Epiphyseal stippling
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal bone structure(HPO:0003330)
                Abnormal bone ossification(HPO:0011849)
                   Abnormal epiphyseal ossification(HPO:0010656)
                      Epiphyseal stippling(HPO:0010655)
                         Neonatal epiphyseal stippling(HPO:0005756)
             Abnormality of long bone morphology(HPO:0011314)
                Abnormality of epiphysis morphology(HPO:0005930)
                   Epiphyseal stippling(HPO:0010655)
                      Neonatal epiphyseal stippling(HPO:0005756)
          Ectopic calcification(HPO:0010766)
             Epiphyseal stippling(HPO:0010655)
                Neonatal epiphyseal stippling(HPO:0005756)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)