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782949007: Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder)


Status: current, Primitive. 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 Case insensitive SNOMED CT core
3756901015 FACES (facial dysmorphism, anorexia, cachexia, eye and skin anomalies) syndrome en Synonym Active Case sensitive SNOMED CT core
3756902010 Friedman Goodman syndrome en Synonym Active Case sensitive SNOMED CT core
3756903017 Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome en Synonym Active Case insensitive SNOMED CT core
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 Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Occurrence Congenital true Inferred relationship Some 3
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Café au lait spots true Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Retinitis pigmentosa true Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Occurrence Congenital true Inferred relationship Some 1
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Occurrence Congenital true Inferred relationship Some 2
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Finding site Retinal structure true Inferred relationship Some 1
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Finding site Skin structure true Inferred relationship Some 3
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Associated morphology Dystrophy true Inferred relationship Some 1
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Finding site Face structure true Inferred relationship Some 2
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Associated morphology Pigment alteration true Inferred relationship Some 3
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome Is a Hereditary disorder of the integument true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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