Oliver McFarlane syndrome 719944006
SNOMED CT code
| SNOMED code | 719944006 |
|---|---|
| name | Oliver McFarlane syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Trichomegaly with retina pigmentary degeneration and dwarfism syndrome (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Ectoderm structure 63206006 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Finding site | Entire eyelashes 367575006 |
| Associated morphology | Abnormally long growth 67946009 |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Pigmentary degeneration 40299004 |
| Finding site | Retinal structure 5665001 |
| attributes - group4 | |
| Interprets | Height / growth measure 271603002 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Hair finding 247522004 Disorder of hair 279425004 Disorder of hair growth 267808001 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Congenital deformity 276655000 Congenital deformity of face 398206004 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Deformity 417893002 Deformity of eyelid 430960001 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Globe finding 246915008 Retina finding 399858007 Retinal disorder 29555009 Congenital anomaly of retina 49381001 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 General finding of soft tissue 248402002 Disorder of soft tissue 19660004 Congenital deformity of soft tissue 673791000119108 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Eyelid finding 246812007 Disorder of eyelid 60113004 Congenital anomaly of eyelid 91158006 Oliver McFarlane syndrome 719944006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disorder of eye 62585004 Degeneration of retina 95695004 Oliver McFarlane syndrome 719944006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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