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700062000: Schöpf-Schulz-Passarge syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2988985014 Schöpf-Schulz-Passarge syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2988996018 Schöpf-Schulz-Passarge syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5457620018 Keratosis palmoplantaris, cystic eyelids, hypodontia, hypotrichosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5457621019 Eccrine tumours ectodermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5457622014 SSPS - Schöpf Schulz Passarge syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5457623016 Eccrine tumors ectodermal dysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5457624010 Palmoplantar hyperkeratosis, cystic eyelids, hypodontia, hypotrichosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5457625011 Palmoplantar keratoderma, cystic eyelids, hypodontia, hypotrichosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5457626012 Schöpf Schulz Passarge syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
871071000172118 SSPS - Schöpf-Schulz-Passarge syndrome fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
943791000172114 syndrome de Schöpf-Schulz-Passarge fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3443961001000110 Schöpf-Schulz-Passarge-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Schöpf-Schulz-Passarge syndrome Is a Hereditary cancer-predisposing syndrome true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Autosomal hereditary disorder true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Occurrence Congenital true Inferred relationship Some 1
Schöpf-Schulz-Passarge syndrome Finding site Ectoderm structure true Inferred relationship Some 1
Schöpf-Schulz-Passarge syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Schöpf-Schulz-Passarge syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Schöpf-Schulz-Passarge syndrome Is a Hereditary disorder of tooth true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Ectodermal dysplasia with hair-tooth-nail defects (disorder) true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Hereditary diffuse palmoplantar keratoderma (disorder) true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Genetic disorder of nail (disorder) true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Hypotrichosis true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Dystrophia unguium true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Occurrence Congenital true Inferred relationship Some 4
Schöpf-Schulz-Passarge syndrome Finding site Nail unit is a complex structure which consists of nail plate, nail bed, nail root and skin around the nail plate. true Inferred relationship Some 4
Schöpf-Schulz-Passarge syndrome Associated morphology Dystrophy true Inferred relationship Some 4
Schöpf-Schulz-Passarge syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Schöpf-Schulz-Passarge syndrome Occurrence Congenital true Inferred relationship Some 6
Schöpf-Schulz-Passarge syndrome Finding site Hair structure (body structure) true Inferred relationship Some 6
Schöpf-Schulz-Passarge syndrome Associated morphology Growth alteration true Inferred relationship Some 6
Schöpf-Schulz-Passarge syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 6
Schöpf-Schulz-Passarge syndrome Finding site Entire skin of palmar area of hand (body structure) true Inferred relationship Some 2
Schöpf-Schulz-Passarge syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 2
Schöpf-Schulz-Passarge syndrome Finding site Entire skin of sole of foot true Inferred relationship Some 3
Schöpf-Schulz-Passarge syndrome Associated morphology Hyperkeratosis true Inferred relationship Some 3
Schöpf-Schulz-Passarge syndrome Is a Hereditary disorder of the visual system true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Congenital anomaly in number of teeth (disorder) true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Is a Cyst of eyelid true Inferred relationship Some
Schöpf-Schulz-Passarge syndrome Occurrence Congenital true Inferred relationship Some 7
Schöpf-Schulz-Passarge syndrome Finding site Tooth structure true Inferred relationship Some 7
Schöpf-Schulz-Passarge syndrome Associated morphology Abnormal number (morphologic abnormality) true Inferred relationship Some 7
Schöpf-Schulz-Passarge syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 7
Schöpf-Schulz-Passarge syndrome Occurrence Congenital true Inferred relationship Some 8
Schöpf-Schulz-Passarge syndrome Finding site Tooth structure true Inferred relationship Some 8
Schöpf-Schulz-Passarge syndrome Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 8
Schöpf-Schulz-Passarge syndrome Finding site Eyelid structure true Inferred relationship Some 5
Schöpf-Schulz-Passarge syndrome Associated morphology Multiple cysts true Inferred relationship Some 5
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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