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Ontology Browser
Term:
nonsyndromic congenital nail disorder (DOID:0080683)
Annotations: Rat: (8) Mouse: (8) Human: (8) Chinchilla: (8) Bonobo: (8) Dog: (8) Squirrel: (7) Pig: (7)
Parent Terms Term With Siblings Child Terms
Malformed Nails +     
physical disorder +     
ADULT syndrome  
agnathia-otocephaly complex  
Alopecia Universalis, Onychodystrophy, Vitiligo 
Ameloonychohypohidrotic Syndrome 
Anonychia Onychodystrophy 
Anonychia with Flexural Pigmentation 
Anonychia-Ectrodactyly 
autosomal dominant congenital deafness with onychodystrophy  
autosomal recessive congenital ichthyosis +   
BASAN syndrome  
bladder exstrophy-epispadias-cloacal exstrophy complex +   
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome 
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
Cartwright Nelson Fryns Syndrome 
caudal regression syndrome  
cleft palate-lateral synechia syndrome  
congenital adrenal hyperplasia +   
congenital adrenal insufficiency  
congenital afibrinogenemia +   
congenital amegakaryocytic thrombocytopenia  
congenital aphakia  
congenital bilateral absence of vas deferens +   
congenital bile acid synthesis defect +   
congenital central hypoventilation syndrome  
congenital chylothorax  
congenital contractural arachnodactyly  
congenital diaphragmatic hernia +   
congenital diarrhea +   
congenital disorder of glycosylation +   
congenital epulis 
congenital fibrosarcoma 
congenital fibrosis of the extraocular muscles +   
Congenital Foot Deformities +   
congenital generalized lipodystrophy +   
congenital granular cell tumor 
congenital heart block +   
congenital heart disease +   
congenital hemolytic anemia +   
congenital hereditary endothelial dystrophy of cornea  
congenital hypogammaglobulinemia 
congenital hypoplastic anemia +   
congenital hypothyroidism +   
congenital hypotrichosis with juvenile macular dystrophy  
congenital intrinsic factor deficiency  
congenital lactase deficiency  
congenital leptin deficiency  
congenital megabladder  
congenital mesoblastic nephroma +   
congenital mirror movement disorder +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
congenital myopathy +   
congenital nervous system abnormality +   
congenital nystagmus +   
congenital ptosis +   
congenital secretory chloride diarrhea 1  
congenital stationary night blindness +   
congenital stromal corneal dystrophy  
congenital structural myopathy +   
congenital sucrase-isomaltase deficiency  
congenital syphilis +  
congenital toxoplasmosis 
cryptophthalmia +   
Curly Hair-Acral Keratoderma-Caries Syndrome 
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
Dermoodontodysplasia 
developmental cardiac valvular defect  
DOORS syndrome  
Double Nail for Fifth Toe 
epidermolysis bullosa with congenital localized absence of skin and deformity of nails  
gastroschisis +   
Gorlin Bushkell Jensen Syndrome 
Heimler syndrome 1  
Hereditary Koilonychia 
hypospadias +   
Hypospadias-Mental Retardation Syndrome 
imperforate anus +   
Klippel-Feil syndrome +   
Kumar Levick Syndrome 
large congenital melanocytic nevus  
laryngomalacia +   
Leber congenital amaurosis +   
lethal congenital contracture syndrome +   
lethal congenital glycogen storage disease of heart  
Mammary-Digital-Nail Syndrome 
Meckel's diverticulum 
MLS syndrome +   
multiple congenital anomalies-hypotonia-seizures syndrome +   
neural tube defect +   
non-congenital cyst of kidney 
nonsyndromic congenital nail disorder +   
A nail disease that is characterized by underdevelopment of nails. (DO)
Oculotrichodysplasia 
omphalocele  
Onychotrichodysplasia and Neutropenia 
orofacial cleft +   
Otoonychoperoneal Syndrome 
palmoplantar keratoderma and congenital alopecia 1  
palmoplantar keratoderma and congenital alopecia 2 
Pili Torti Onychodysplasia 
Pinheiro Freire-Maia Miranda Syndrome 
Poland syndrome 
polydactyly +   
primary congenital glaucoma +   
radioulnar synostosis +   
rapidly involuting congenital hemangioma 
Santos Syndrome 
Schinzel-Giedion Syndrome  
severe congenital encephalopathy due to MECP2 mutation  
severe congenital neutropenia +   
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
Silver-Russell syndrome +   
spondyloepiphyseal dysplasia with congenital joint dislocations  
Steatocystoma Multiplex with Natal Teeth 
T-cell immunodeficiency, congenital alopecia, and nail dystrophy  
Teebi Kaurah Syndrome 
Temple-Baraitser syndrome  
Tonoki Syndrome 
tooth and nail syndrome  
TORCH syndrome 
Total Anonychia with Microcephaly 
Ulnar Hypoplasia with Mental Retardation 
visceral heterotaxy +   
yellow nail syndrome +  
Zika virus congenital syndrome 
Zori Stalker Williams Syndrome 

Synonyms
Xrefs: OMIM:PS161050
Definition Sources: https://pubmed.ncbi.nlm.nih.gov/26149975/ "DO"

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