62192003: Diprosopus (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Finding of face\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Diprosopus
\Head finding (finding)\Disorder of head (disorder)\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Diprosopus
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of face (disorder)\Diprosopus

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Diprosopus
\Disease\Disorder of head (disorder)\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Diprosopus
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of face (disorder)\Diprosopus
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Diprosopus

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

103356013 Diprosopus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

103358014 Monocephalus diprosopus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

801337019 Diprosopus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1793121000005114 Diprosopus da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Diprosopus	Is a	misfoster	false	Inferred relationship	Some
Diprosopus	Finding site	Fetal structure	false	Inferred relationship	Some
Diprosopus	Occurrence	Fetal period	false	Inferred relationship	Some
Diprosopus	Occurrence	Congenital	false	Inferred relationship	Some
Diprosopus	Associated morphology	Kongenit malformation	false	Inferred relationship	Some
Diprosopus	Occurrence	Congenital	true	Inferred relationship	Some	1
Diprosopus	Associated morphology	dysgenese	false	Inferred relationship	Some	1
Diprosopus	Finding site	Fetal structure	false	Inferred relationship	Some	1
Diprosopus	Is a	Congenital anomaly of face (disorder)	true	Inferred relationship	Some
Diprosopus	Associated morphology	Double structure (morphologic abnormality)	false	Inferred relationship	Some	2
Diprosopus	Occurrence	Congenital	false	Inferred relationship	Some	2
Diprosopus	Finding site	Face structure	false	Inferred relationship	Some	2
Diprosopus	Finding site	Face structure	true	Inferred relationship	Some	1
Diprosopus	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Diprosopus	Associated morphology	Double structure (morphologic abnormality)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cephalodiprosopus	Is a	True	Diprosopus	Inferred relationship	Some
Diprosopus tetrophthalmus	Is a	True	Diprosopus	Inferred relationship	Some
Opodidymus	Is a	True	Diprosopus	Inferred relationship	Some
Janiceps	Is a	True	Diprosopus	Inferred relationship	Some
Congenital double lip	Is a	True	Diprosopus	Inferred relationship	Some
A rare, major congenital malformation characterized by complete duplication of the nose resulting in two fully developed noses often associated with choanal atresia, causing respiratory distress and necessitating surgical repair.	Is a	True	Diprosopus	Inferred relationship	Some
Eyebrow duplication-syndactyly syndrome is characterized by partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes, and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive.	Is a	True	Diprosopus	Inferred relationship	Some
Distichiasis	Is a	False	Diprosopus	Inferred relationship	Some
Congenital distichiasis	Is a	True	Diprosopus	Inferred relationship	Some

Reference Sets