loading...| Preferred Name |
achromatopsia |
|
| Synonyms |
Monochromatism ACHM |
|
| Definitions |
A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_13911 |
|
| alternative label |
Monochromatism ACHM |
|
| database_cross_reference |
ICD9CM:368.54 ICD10CM:H53.51 SNOMEDCT_US_2023_03_01:56852002 UMLS_CUI:C0152200 MESH:D003117 NCI:C84528 ORDO:49382 |
|
| definition |
A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. |
|
| has exact synonym |
Monochromatism ACHM |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:13911 |
|
| in_subset | ||
| label |
achromatopsia |
|
| notation |
DOID:13911 |
|
| note |
A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance. |
|
| preferred label |
achromatopsia |
|
| prefLabel |
achromatopsia |
|
| subClassOf |