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Sclerotic radial metaphysis with longitudinal striations

MedGen UID:: 870975
•Concept ID:: C4025438
•: Anatomical Abnormality

HPO:	HP:0004022

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVSclerotic radial metaphysis with longitudinal striations

Phenotypic abnormality
- Abnormality of limbs
  - Abnormality of the upper limb
    - Abnormal upper limb metaphysis morphology
      - Abnormal radial metaphysis morphology
        Sclerotic radial metaphysis with longitudinal striations

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Sclerotic radial metaphysis with longitudinal striations
Sclerotic radial metaphysis with longitudinal striations

MedGen
IMMP2L inner mitochondrial membrane peptidase subunit 2 [Homo sapiens]
IMMP2L inner mitochondrial membrane peptidase subunit 2 [Homo sapiens]
Gene ID:83943

Gene
Gene Links for dbVar (Select 46797171) (1)
Gene
Congenital disorder of glycosylation type I
Congenital disorder of glycosylation type I

MedGen
C4700504[conceptid] (1)
MedGen

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