Coarse hair

Symptom Information:

Symptom ID: HPO:0002208
Synonyms:
Coarse hair (finding) [Orphanet:24600]
Coarse hair [Orphanet:24600]
Coarse hair [OMIM:Coarse hair]
Coarse/thick hair [Orphanet:24600]
Coarse hair (in some patients) [OMIM:Coarse hair (in some patients)]
Thick coarse hair [OMIM:Thick coarse hair]
Quality:
Cross references:
Orphanet:24600 "Coarse/thick hair" [Orphanet:24600]
OMIM: "Coarse hair" [OMIM:Coarse hair]
OMIM: "Coarse hair (in some patients)" [OMIM:Coarse hair (in some patients)]
OMIM: "Thick coarse hair" [OMIM:Thick coarse hair]
UMLS:C0277959 "Coarse hair" [Orphanet:24600]
Is a (Direct Parents):
HPO         Abnormality of hair texture
Orphanet Abnormality of hair texture
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormality of hair texture(HPO:0010719)
                   Coarse hair(HPO:0002208)
MedDRA:
Database Frequency: 58 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Acroosteolysis, dominant type (Orphanet:955)
Amaurosis - hypertrichosis (Orphanet:1021)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Argininosuccinic aciduria (Orphanet:23)
Autosomal dominant chondrodysplasia punctata (Orphanet:79344)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Björnstad syndrome (Orphanet:123)
Bohring-Opitz syndrome (Orphanet:97297)
Brain malformation - congenital heart disease - postaxial polydactyly (Orphanet:75389)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Coffin-Lowry syndrome (Orphanet:192)
Cohen syndrome (Orphanet:193)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Craniolenticulosutural dysplasia (Orphanet:50814)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia - sensorineural deafness (Orphanet:1883)
Emery-Nelson syndrome (Orphanet:1927)
Fetal hydantoin syndrome (Orphanet:1912)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
HYPOTRICHOSIS 8 (OMIM:278150)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hall-Riggs syndrome (Orphanet:2107)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hurler-Scheie syndrome (Orphanet:93476)
Hypotrichosis simplex (Orphanet:55654)
Incontinentia pigmenti (Orphanet:464)
MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGEDAPPEARANCE (OMIM:248010)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Marie Unna hereditary hypotrichosis (Orphanet:444)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Multiple sulfatase deficiency (Orphanet:585)
Noonan syndrome (Orphanet:648)
ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR (OMIM:164680)
Occipital horn syndrome (Orphanet:198)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Pili torti (Orphanet:2889)
Rabson-Mendenhall syndrome (Orphanet:769)
SENER SYNDROME (OMIM:606156)
Sanfilippo syndrome type A (Orphanet:79269)
Sanfilippo syndrome type B (Orphanet:79270)
Sanfilippo syndrome type C (Orphanet:79271)
Sanfilippo syndrome type D (Orphanet:79272)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Shoulder and girdle defects - familial intellectual deficit (Orphanet:2580)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Trichodysplasia - xeroderma (Orphanet:3361)
Uncombable hair syndrome (Orphanet:1410)
WOOLLY HAIR, AUTOSOMAL DOMINANT (OMIM:194300)
Woolly hair (Orphanet:170)