Disease Browser
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Parent Node:
Corneal Dystrophies, Hereditary (D003317) | Parent Node:
Nail Diseases (D009260) | ..Starting node .. Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia (C565591)
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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 SIMPLEX WITH NAIL DYSTROPHY (OMIM:616487)
| .. 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 1, PHOTOSENSITIVE (OMIM:601675)
| .. Twenty-Nail Dystrophy (C562907)
| .. Yellow Nail Syndrome (D056684) 1
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 4156 |
Name: | Endothelial Dystrophy, Congenital Hereditary, with Nail Hypoplasia |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D003317|MESH:D009260 |
TreeNumbers: | C11.204.236/C565591 |C11.270.162/C565591 |C16.320.290.162/C565591 |C17.800.529/C565591 |
Synonyms: | |
Slim Mappings: | Eye disease|Genetic disease (inborn)|Skin disease |
Reference: |
MedGen: C565591
MeSH: C565591
OMIM: MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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