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Pyknoachondrogenesis (MONDO:0009942)

Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterized by severe generalized osteosclerosis.

Overview

Category

Ontology ID

Internal:11143

Synonyms

camera syndrome

pyknoachondrogenesis

association of skeletal defects resembling achondrogenesis with generalised bone sclerosis

association of skeletal defects resembling achondrogenesis with generalized bone sclerosis

Mapped terms

GARD:0004610

MEDGEN:337844

MESH:C536251

OMIM:265880

Orphanet:3003

SCTID:719258003

UMLS:C1849523

icd11.foundation:588435239

Child terms

Unknown children.