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Diseases

Metaphyseal Chondrodysplasia, Schmid Type

metaphyseal chondrodysplasia, schmid type

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

Grouped by core information, identifiers, and descriptions.

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Core Information

Disease Name
Metaphyseal Chondrodysplasia, Schmid Type
Standard Disease Name
metaphyseal chondrodysplasia, schmid type
MeSH Tree
No data
ICD-10
Q78.5

Identifiers

DO ID
No data
MeSH ID
C537352
OMIM ID
156500
UMLS ID
C0265289
HPO ID
No data

Description and Extensions

Description
Schmid metaphyseal chondrodysplasia is a rare disorder characterized by moderately short stature with short limbs, coxa vara, bowlegs and an abnormal gait.
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease8 Targets
02
CEBPB
CCAAT enhancer binding protein beta
CCAAT enhancer binding protein beta
08
RUNX2
RUNX family transcription factor 2
RUNX family transcription factor 2