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239035009: Ectodermal dysplasia with hair-nail defect (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
358219010 Ectodermal dysplasia with hair-nail defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
627996018 Ectodermal dysplasia with hair-nail defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5026771000241116 dysplasie ectodermique avec déficit de cheveux-ongles fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3437191001000112 Dysplasie, ektodermale, reiner Haar-Nagel-Typ de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


45 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ectodermal dysplasia with hair-nail defect Is a Ectodermal dysplasia false Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Associated morphology Dysplasia false Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Occurrence Congenital false Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Finding site Skin structure false Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Associated morphology anomalie congénitale false Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Finding site Skin structure false Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Finding site Skin structure false Inferred relationship Some 2
Ectodermal dysplasia with hair-nail defect Occurrence Congenital true Inferred relationship Some 2
Ectodermal dysplasia with hair-nail defect Associated morphology anomalie du développement false Inferred relationship Some 2
Ectodermal dysplasia with hair-nail defect Occurrence Congenital true Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Associated morphology Congenital dysplasia false Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Is a Congenital anomaly of nail false Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Is a Congenital anomaly of hair true Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Finding site Ectoderm structure true Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Occurrence Congenital false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Occurrence Congenital false Inferred relationship Some 5
Ectodermal dysplasia with hair-nail defect Associated morphology anomalie du développement false Inferred relationship Some 5
Ectodermal dysplasia with hair-nail defect Finding site Hair structure (body structure) false Inferred relationship Some 5
Ectodermal dysplasia with hair-nail defect Associated morphology anomalie du développement false Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Finding site Nail structure false Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Associated morphology Congenital dysplasia false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Finding site Ectoderm structure false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Finding site Skin structure false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Ectodermal dysplasia with hair-nail defect Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Ectodermal dysplasia with hair-nail defect Occurrence Congenital true Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Pathological process (attribute) Pathological developmental process false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Associated morphology Morphologically abnormal structure false Inferred relationship Some 4
Ectodermal dysplasia with hair-nail defect Finding site Hair structure (body structure) true Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Ectodermal dysplasia with hair-nail defect 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 2
Ectodermal dysplasia with hair-nail defect Is a Disorder of nail (disorder) false Inferred relationship Some
Ectodermal dysplasia with hair-nail defect Associated morphology Dysplasia true Inferred relationship Some 3
Ectodermal dysplasia with hair-nail defect Is a Ectodermal dysplasia with nail defect true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Tricho-oculodermovertebral syndrome Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Curly hair, ankyloblepharon, nail dysplasia syndrome (disorder) Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Hidrotic ectodermal dysplasia, Halal type is a form of ectodermal dysplasia syndrome characterized by trichodysplasia, with absent eyebrows and eyelashes, onychodysplasia, mild retrognathia, abnormal dermatoglyphics (excess of whorls on fingertips, radial loop on finger, hypothenar pattern), intellectual disability and normal teeth and sweating. Additional variable manifestations include high implanted or prominent ears, mild hearing loss, supernumerary nipple, café-au-lait spots, keratosis pilaris, and irregular menses. To date, four individuals from 2 generations of a consanguineous family of Portuguese descent have been described in the literature. Males and females were equally affected. Hidrotic ectodermal dysplasia, Halal type is inherited in an autosomal recessive manner. Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
A rare ectodermal dysplasia syndrome characterized by congenital onychodystrophy (particularly of the distal nail) and severe hypotrichosis with alopecia involving the eyebrows, eyelashes and body hair. Scalp, beard, pubic and axillary hair is brittle and shows a twisting pattern on electron microscopy. There have been no further descriptions in the literature since 1991. Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Trichodermodysplasia-dental alterations syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by sparse, thin, brittle scalp hair, as well as sparse eyebrows, eyelashes, axillary and pubic hair, delayed eruption of deciduous teeth and hypodontia of both dentitions. Mild palmoplantar keratosis, café-au-lait spots on back, mild dystrophy of nails, and tibial deflection of toes are also associated. There have been no further descriptions in the literature since 1986. Is a False Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Odonto-onycho dysplasia-alopecia syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by almost total alopecia with only sparse, thin, brittle, slow-growing scalp hair, fair and sparse eyebrows and eyelashes, absent axillary and pubic hair, fragile and brittle fingernails, thick and brittle toenails (both with a subungual corneal layer), hypodontia, microdontia, widely spaced teeth with hypoplastic enamel, mild palmoplantar keratosis, café-au-lait spots and areolae anomalies. There have been no further descriptions in the literature since 1985. Is a False Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Hidrotic ectodermal dysplasia, Christianson-Fourie type is a rare ectodermal dysplasia syndrome characterized by tricho- and onychodysplasia in association with cardiac rhythm abnormalities. Patients present with sparse scalp hair and eyelashes, absent or sparse eyebrows, dystrophic thickened nails (on fingers distal end may be lifted from the nail bed) and supraventricular tachycardia or sinus bradycardia. Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
A rare, genetic, ectodermal dysplasia syndrome characterized by skin, hair and nail anomalies (i.e. generalized ichthyosis, congenital alopecia universalis, dystrophic, convex nails), associated with hypohidrosis without hyperthermia, intellectual disability, seizures, and skeletal (e.g. proportionate short stature, platyspondyly) and intestinal (e.g. congenital aganglionic megacolon) anomalies. Facial dysmorphism includes frontal bossing, blepharophimosis, large ears, low nasal bridge and small nose. There have been no further descriptions in the literature since 1992. Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Ectodermal dysplasia with hair-tooth-nail defects (disorder) Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
Hidrotic ectodermal dysplasia syndrome Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some
A rare genetic skin disease characterised by infantile onset of diffuse alopecia, abnormal skin pigmentation (hypo- and hyperpigmented macules of the trunk and face and areas of reticular hypo- and hyperpigmentation of the extremities), palmoplantar keratoderma, and nail dystrophy. Patients develop recurrent spinocellular carcinomas later in life. Brittle teeth resulting in early loss of dentition have also been described. Is a True Ectodermal dysplasia with hair-nail defect Inferred relationship Some

This concept is not in any reference sets

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