3944006: Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female (disorder)

SNOMED CT Concept\Clinical finding\...

\Pregnancy, childbirth and puerperium finding\Finding of structures of conception\Placental finding\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Pregnancy, childbirth and puerperium finding\Finding of structures of conception\Placental finding\Finding of placental function\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Pregnancy, childbirth and puerperium finding\Complication of pregnancy, childbirth and/or puerperium\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Pregnancy, childbirth and puerperium finding\Finding related to pregnancy\Disorder of pregnancy\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Pregnancy, childbirth and puerperium finding\Finding related to pregnancy\Placental finding\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Pregnancy, childbirth and puerperium finding\Finding related to pregnancy\Placental finding\Finding of placental function\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency

\Functional finding\Finding of placental function\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency

\Endocrine finding\Disorder of placental endocrine function\Placental sulfatase deficiency

\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\Placental sulfatase deficiency
\Disease\Complication of pregnancy, childbirth and/or puerperium\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Disease\Disorder of pregnancy\Disorder of placenta\Deficiency of placental function\Disorder of placental endocrine function\Placental sulfatase deficiency
\Disease\Metabolic disease\Enzymopathy\Deficiency of steryl-sulfatase\Placental sulfatase deficiency
\Disease\Metabolic disease\Disorder of steroid metabolism\Placental sulfatase deficiency

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

194882017 X-linked placental steryl-sulfatase deficiency en Synonym Active Case sensitive SNOMED CT core
2772402017 Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female en Synonym Active Initial character case insensitive SNOMED CT core
492078016 X-linked recessive ichthyosis en Synonym Inactive Case sensitive SNOMED CT core
492079012 XRI - X-linked recessive ichthyosis en Synonym Inactive Case sensitive SNOMED CT core
492080010 Placental steroidal sulphatase deficiency en Synonym Active Case insensitive SNOMED CT core
492081014 Steroid sulphatase deficiency en Synonym Active Case insensitive SNOMED CT core
492082019 Placental sulphatase deficiency en Synonym Active Case insensitive SNOMED CT core
492083012 X-linked placental steryl-sulphatase deficiency en Synonym Active Case sensitive SNOMED CT core
775893013 Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
8574013 Steryl-sulfatase deficiency en Synonym Inactive Initial character case insensitive SNOMED CT core
8575014 Steroid sulfatase deficiency en Synonym Active Case insensitive SNOMED CT core
8576010 X-linked ichthyosis en Synonym Inactive Case sensitive SNOMED CT core
8577018 Placental sulfatase deficiency en Synonym Active Case insensitive SNOMED CT core
8578011 SSDD en Synonym Inactive Initial character case insensitive SNOMED CT core
8579015 Steroid sulfatase deficiency disease en Synonym Inactive Initial character case insensitive SNOMED CT core
8580017 STS en Synonym Inactive Initial character case insensitive SNOMED CT core
8581018 Placental steroidal sulfatase deficiency en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Placental sulfatase deficiency	Interprets	Pregnancy observable	false	Inferred relationship	Some	2
Placental sulfatase deficiency	Occurrence	Maternal pregnancy period	false	Inferred relationship	Some	3
Placental sulfatase deficiency	Occurrence	Maternal pregnancy period	true	Inferred relationship	Some	2
Placental sulfatase deficiency	Interprets	Placental endocrine function	true	Inferred relationship	Some	1
Placental sulfatase deficiency	Finding site	Placental structure	true	Inferred relationship	Some	2
Placental sulfatase deficiency	Has interpretation	Deficient	true	Inferred relationship	Some	1
Placental sulfatase deficiency	Is a	Disorder of steroid metabolism	true	Inferred relationship	Some
Placental sulfatase deficiency	Is a	Reproductive system hereditary disorder	false	Inferred relationship	Some
Placental sulfatase deficiency	Is a	X-linked hereditary disease	true	Inferred relationship	Some
Placental sulfatase deficiency	Is a	Disorder of placental endocrine function	true	Inferred relationship	Some
Placental sulfatase deficiency	Is a	Deficiency of steryl-sulfatase	true	Inferred relationship	Some
Placental sulfatase deficiency	Finding site	Placental structure	false	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
194882017	X-linked placental steryl-sulfatase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
2772402017	Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
492078016	X-linked recessive ichthyosis	en	Synonym	Inactive	Case sensitive	SNOMED CT core
492079012	XRI - X-linked recessive ichthyosis	en	Synonym	Inactive	Case sensitive	SNOMED CT core
492080010	Placental steroidal sulphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
492081014	Steroid sulphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
492082019	Placental sulphatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
492083012	X-linked placental steryl-sulphatase deficiency	en	Synonym	Active	Case sensitive	SNOMED CT core
775893013	Placental sulfatase deficiency (X-linked steryl-sulfatase deficiency) in a female (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
8574013	Steryl-sulfatase deficiency	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
8575014	Steroid sulfatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
8576010	X-linked ichthyosis	en	Synonym	Inactive	Case sensitive	SNOMED CT core
8577018	Placental sulfatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core
8578011	SSDD	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
8579015	Steroid sulfatase deficiency disease	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
8580017	STS	en	Synonym	Inactive	Initial character case insensitive	SNOMED CT core
8581018	Placental steroidal sulfatase deficiency	en	Synonym	Active	Case insensitive	SNOMED CT core