Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Hair Diseases (D006201)
..Starting node
..expand
Catatrichy (C535346)

       Child Nodes:



 Sister Nodes: 
..expandBamforth syndrome (C537901)
..expandBird headed dwarfism Montreal type (C535448)
..expandBjornstad syndrome (C537633)
..expandCardiomyopathy dilated with Woolly hair and keratoderma (C535581)
..expandCatatrichy (C535346)
..expandCopper deficiency, familial benign (C535468)
..expandCurly hair-ankyloblepharon-nail dysplasia syndrome (C538074)
..expandDermoodontodysplasia (C565103)
..expandECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
..expandFLOTCH syndrome (C537065)
..expandFolliculitis (D005499) Child2
..expandGiedion syndrome (C536820)
..expandHairy palms and soles (C535620)
..expandHirsutism (D006628) Child6
..expandHypertrichosis (D006983) Child27
..expandHypotrichosis (D007039) Child89
..expandKaler Garrity Stern syndrome (C537706)
..expandKatsantoni Papadakou Lagoyanni syndrome (C537012)
..expandKozlowski-Krajewska syndrome (C537615)
..expandMartinez Monasterio Pinheiro syndrome (C536027)
..expandMenkes Kinky Hair Syndrome (D007706) Child1
..expandMonilethrix (D056734) Child1
..expandNaxos disease (C538346)
..expandOculotrichodysplasia (C564934)
..expandOnychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
..expandPiedra (D010854)
..expandPili annulati (C537187)
..expandPili multigemini (C537188)
..expandPili Torti (C562485)
..expandPili torti developmental delay neurological abnormalities (C537398)
..expandPili torti onychodysplasia (C537399)
..expandPseudofolliculitis Barbae (C563016)
..expandPseudomonilethrix (C562988)
..expandRodrigues blindness (C535865)
..expandSkin Fragility-Woolly Hair Syndrome (C564359)
..expandTrichilemmal Cyst 1 (C566458)
..expandTricho-dento-osseous syndrome (C536549)
..expandTricho-dento-osseous syndrome 1 (C536550)
..expandTRICHODENTOOSSEOUS SYNDROME (OMIM:190320)
..expandTrichodysplasia-Xeroderma (C566032)
..expandTrichohepatoenteric Syndrome (C565627)
..expandTrichorhinophalangeal Syndrome, Type III (C566033)
..expandTrichostasis spinulosa (C536558)
..expandTRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH (OMIM:601675)
..expandUncombable hair syndrome (C536939)
..expandWhite forelock with malformations (C536700)
..expandWOOLLY HAIR, AUTOSOMAL DOMINANT (OMIM:194300)
..expandWoolly Hair, Autosomal Recessive (C564735)
..expandWoolly hair, congenital (C536745)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:1872
Name:Catatrichy
Definition:
Alternative IDs:
ParentIDs:MESH:D006201
TreeNumbers:C17.800.329/C535346
Synonyms:Forelock
Slim Mappings:Skin disease
Reference: MedGen: C535346
MeSH: C535346
OMIM: 116850;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0001595Abnormal hair morphology
Disease Causing ClinVar Variants