loading...| Preferred Name | acromicric dysplasia | |
| Synonyms |
ACMICD acromicric skeletal dysplasia |
|
| Definitions |
An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_0111243 |
|
| database_cross_reference |
MESH:C535662 UMLS_CUI:C0265287 SNOMEDCT_US_2023_03_01:254090007 GARD:7 MIM:102370 ORDO:969 |
|
| definition |
An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1. |
|
| has exact synonym |
ACMICD acromicric skeletal dysplasia |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0111243 |
|
| in_subset | ||
| label |
acromicric dysplasia |
|
| notation |
DOID:0111243 |
|
| prefLabel |
acromicric dysplasia |
|
| subClassOf |