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721084001: Deaf blind hypopigmentation syndrome Yemenite type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3323402016 Deaf blind hypopigmentation syndrome Yemenite type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323403014 Deaf blind hypopigmentation syndrome Yemenite type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323404015 Warburg Thomsen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323405019 An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as having cutaneous patchy hypo and hyperpigmentation on the trunk and extremities, grey hair, white brows and lashes. Ocular manifestations were microcornea, coloboma and abnormalities of the anterior chamber of the eye. Both patients had severe hearing loss and dental abnormalities. Intelligence was reported to be normal. Their parents were unaffected and possibly consanguineous. The cause of this syndrome has not been determined. The inheritance pattern appears to be autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3777415016 An exceedingly rare genetic disorder with characteristics of cutaneous pigmentation anomalies, ocular disorders and hearing loss. The syndrome was described in 1990 in two patients from the same Yemenite family. A brother and sister were described as having cutaneous patchy hypo and hyperpigmentation on the trunk and extremities, gray hair, white brows and lashes. Ocular manifestations were microcornea, coloboma and abnormalities of the anterior chamber of the eye. Both patients had severe hearing loss and dental abnormalities. Intelligence was reported to be normal. Their parents were unaffected and possibly consanguineous. The cause of this syndrome has not been determined. The inheritance pattern appears to be autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Congenital deficiency of pigment of skin true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Congenital anomaly of eye true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Auditory system hereditary disorder true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Ear structure false Inferred relationship Some 3
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Occurrence Congenital false Inferred relationship Some 3
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Occurrence Congenital false Inferred relationship Some 4
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Associated morphology dysgenese false Inferred relationship Some 3
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Eye structure false Inferred relationship Some 3
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Associated morphology Kongenit hypopigmentering false Inferred relationship Some 4
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Skin structure false Inferred relationship Some 4
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Genetic disorder of skin pigmentation (disorder) true Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Occurrence Congenital true Inferred relationship Some 1
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Skin structure true Inferred relationship Some 2
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Occurrence Congenital true Inferred relationship Some 2
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Eye structure true Inferred relationship Some 1
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Associated morphology Hypopigmentation true Inferred relationship Some 2
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Congenital hearing disorder false Inferred relationship Some
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Interprets Hearing true Inferred relationship Some 4
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Some 3
Deaf blind hypopigmentation syndrome Yemenite type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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