Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHair Diseases (D006201)
..Starting node
..expandHypertrichosis (D006983)

       Child Nodes:
........expandAcromegaloid facial appearance syndrome (C535655)
........expandAmaurosis hypertrichosis (C536604)
........expandAmbras syndrome (C536605)
........expandBarber Say syndrome (C537908)
........expandCAHMR syndrome (C537959)
........expandCantu syndrome (C535572)
........expandCervical hypertrichosis neuropathy (C537956)
........expandCervical Hypertrichosis with Underlying Kyphoscoliosis (C566142)
........expandCongenital hypertrichosis lanuginosa (C538389)
........expandFacial Hypertrichosis (C565029)
........expandFibromatosis, Gingival, with Hypertrichosis and Mental Retardation (C565331)
........expandGorlin Chaudhry Moss syndrome (C537290)
........expandHairy Ears (C562484)
........expandHairy Ears, Y-Linked (C564029)
........expandHairy elbows (C535618)
........expandHairy nose tip (C535619)
........expandHypertrichosis congenital generalized X-linked (C538388)
........expandHypertrichosis Terminalis, Generalized, with or without Gingival Hyperplasia (C565016)
........expandHypertrichosis, anterior cervical (C538390)
........expandHypertrichosis, Congenital Anterior Cervical, with Peripheral Sensory and Motor Neuropathy (C565492)
........expandHypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features (C538391)
........expandMidphalangeal hair (C537471)
........expandMuller Barth Menger syndrome (C537370)
........expandOliver-McFarlane syndrome (C536554)
........expandRamon Syndrome (C535285)
........expandSchaap Taylor Baraitser syndrome (C536626)
........expandWiedemann Grosse Dibbern syndrome (C536704)



 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:5507
Name:Hypertrichosis
Definition:Excessive hair growth at inappropriate locations, such as on the extremities, the head, and the back. It is caused by genetic or acquired factors, and is an androgen-independent process. This concept does not include HIRSUTISM which is an androgen-dependent excess hair growth in WOMEN and CHILDREN.
Alternative IDs:
ParentIDs:MESH:D006201
TreeNumbers:C17.800.329.875
Synonyms:Hypertrichoses
Slim Mappings:Skin disease
Reference: MedGen: D006983
MeSH: D006983
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants