| Disease Browser
|
Parent Node:
 Bone Diseases, Developmental (D001848) | Parent Node:
Dental Enamel Hypoplasia (D003744) | Parent Node:
Ectodermal Dysplasia (D004476) | Parent Node:
Hypotrichosis (D007039) | Parent Node:
Nail Diseases (D009260) | ..Starting node
.. Trichoodontoonychial Dysplasia (C564760)
|
Child Nodes:
|
Sister Nodes: | ..Al Gazali Hirschsprung syndrome (C535615)
| ..Basaran Yilmaz syndrome (C537660)
| ..Brachydactyly type A5 nail dysplasia (C537091)
| ..Candidiasis, Familial, 3 (C564361)
| ..Dermatopathia pigmentosa reticularis (C535374)
| ..Double Nail for Fifth Toe (C565090)
| ..ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
| ..Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia (C565591)
| ..Epidermolysis bullosa, late-onset localized junctional, with mental retardation (C535492)
| ..FLOTCH syndrome (C537065)
| ..Hooft disease (C535329)
| ..Judge Misch Wright syndrome (C537692)
| ..Keratoderma palmoplantar spastic paralysis (C536153)
| ..Leukonychia totalis (C535889)
| ..Nail dysplasia, isolated congenital (C538333)
| ..Nail-Patella Syndrome (D009261)  1
| ..Nails, Ingrown (D009263)
| ..Odontomicronychial dysplasia (C537741)
| ..Onychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
| ..Onycholysis (D054039) 3
| ..Onychomycosis (D014009)
| ..Pachyonychia Congenita (D053549) 5
| ..Paronychia (D010304)
| ..Patel Bixler syndrome (C536306)
| ..Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails (C563941)
| ..Subungual exostoses (C535723)
| ..T-cell immunodeficiency, congenital alopecia and nail dystrophy (C536781)
| ..Toenail Dystrophy, Isolated (C564384)
| ..Trichoodontoonychial Dysplasia (C564760)
| ..TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675)
| ..Twenty-Nail Dystrophy (C562907)
| ..Yellow Nail Syndrome (D056684) 1
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
|
|
| Term ID: | 11238 |
| Name: | Trichoodontoonychial Dysplasia |
| Definition: | |
| Alternative IDs: | |
| ParentIDs: | MESH:D001848|MESH:D003744|MESH:D004476|MESH:D007039|MESH:D009260 |
| TreeNumbers: | C05.116.099/C564760 |C07.650.800.255/C564760 |C07.793.700.255/C564760 |C16.131.077.350/C564760 |C16.131.831.350/C564760 |C16.131.850.800.255/C564760 |C16.320.850.250/C564760 |C17.800.329.937/C564760 |C17.800.529/C564760 |C17.800.804.350/C564760 |C17.800.827.250/C5 |
| Synonyms: | |
| Slim Mappings: | Congenital abnormality|Genetic disease (inborn)|Mouth disease|Musculoskeletal disease|Skin disease |
| Reference: |
MedGen: C564760
MeSH: C564760
OMIM: 275450;
Genes: | | Phenotypes | | | Disease Causing ClinVar Variants | |
|
