Fine hair

Symptom Information:

Symptom ID: HPO:0002213
Synonyms:
Fine hair (finding) [Orphanet:24560]
Fine hair [Orphanet:24560]
Fine hair [OMIM:Fine hair]
Fine hair (in some patients) [OMIM:Fine hair (in some patients)]
Quality:
Cross references:
Orphanet:24560 "Fine hair" [Orphanet:24560]
OMIM: "Fine hair" [OMIM:Fine hair]
OMIM: "Fine hair (in some patients)" [OMIM:Fine hair (in some patients)]
UMLS:C0423867 "Fine hair" [Orphanet:24560]
Is a (Direct Parents):
Orphanet Abnormality of hair texture
HPO         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)
                   Fine hair(HPO:0002213)
MedDRA:
Database Frequency: 77 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q32q33 microdeletion syndrome (Orphanet:251019)
ACROKERATODERMA, HEREDITARY PAPULOTRANSLUCENT (OMIM:101840)
ADULT syndrome (Orphanet:978)
ANGIOMA SERPIGINOSUM, X-LINKED (OMIM:300652)
Ablepharon macrostomia syndrome (Orphanet:920)
Acquired hypertrichosis lanuginosa (Orphanet:2221)
Acrogeria (Orphanet:2500)
Acromelanosis (Orphanet:39)
Amelo-onycho-hypohidrotic syndrome (Orphanet:1028)
Atypical Rett syndrome (Orphanet:3095)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Choroidal atrophy - alopecia (Orphanet:1433)
Cockayne syndrome (Orphanet:191)
Conductive deafness - ptosis - skeletal anomalies (Orphanet:3236)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Crandall syndrome (Orphanet:202)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 3 (OMIM:614099)
Distal trisomy 6p (Orphanet:1745)
Dubowitz syndrome (Orphanet:235)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Ectodermal dysplasia syndrome (Orphanet:79373)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Genitopatellar syndrome (Orphanet:85201)
Growth hormone insensitivity syndrome (Orphanet:181393)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hallermann-Streiff syndrome (Orphanet:2108)
Hawkinsinuria (Orphanet:2118)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Hypodontia - dysplasia of nails (Orphanet:2228)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Isolated sulfite oxidase deficiency (Orphanet:99731)
KID syndrome (Orphanet:477)
Lysinuric protein intolerance (Orphanet:470)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Monilethrix (Orphanet:573)
Mowat-Wilson syndrome (Orphanet:2152)
Myhre syndrome (Orphanet:2588)
Netherton syndrome (Orphanet:634)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
RAPP-HODGKIN SYNDROME (OMIM:129400)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Ringed hair disease (Orphanet:169)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Short-limb skeletal dysplasia with severe combined immunodeficiency (Orphanet:935)
Syndromic diarrhea (Orphanet:84064)
Teebi-Shaltout syndrome (Orphanet:3291)
Trichodental syndrome (Orphanet:3351)
Trichodermal syndrome - intellectual deficit (Orphanet:3360)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Weaver syndrome (Orphanet:3447)
Woodhouse-Sakati syndrome (Orphanet:3464)
Woolly hair (Orphanet:170)
Zunich-Kaye syndrome (Orphanet:3474)