Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3756900019 | Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3756901015 | FACES (facial dysmorphism, anorexia, cachexia, eye and skin anomalies) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3756902010 | Friedman Goodman syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3756903017 | Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
8445851000146110 | syndroom van faciale dysmorfie, anorexie, cachexie en afwijkingen van oog en huid | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8445861000146113 | syndroom van faciale dysmorfie, anorexie, cachexie en afwijkingen van oog en huid (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8445871000146119 | syndroom van congenitale afwijking van aangezicht, anorexie, cachexie en afwijkingen van oog en huid | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
8731361000146112 | FACES-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
3756904011 | A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of facial dysmorphism (mild eyelid ptosis, xanthelasma, anteverted nostrils, bifid nasal tip, short palate), severe muscle wasting and cachexia, retinitis pigmentosa, numerous lentigines and cafe-au-lait spots, as well as mild soft tissue syndactyly. Additional features include nasal speech, chest asymmetry, pectus excavatum, genu varum, pes planus, and thyroid papillary carcinoma and diffuse enlargement. There has been no further description in the literature since 1984. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 3 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Café au lait spots | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Retinitis pigmentosa | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Multiple malformation syndrome with facial defects as major feature | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Genetic disorder of skin pigmentation (disorder) | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Finding site | Retinal structure | true | Inferred relationship | Some | 1 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 3 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Finding site | Face structure | true | Inferred relationship | Some | 2 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Associated morphology | Morphologically abnormal structure (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Associated morphology | Pigment alteration | true | Inferred relationship | Some | 3 | |
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) | Is a | Disorder involving the integument of fetus OR newborn | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets