Sparse scalp hair

Symptom Information:

Symptom ID: HPO:0002209
Synonyms:
Scalp hair, thinning [HPO:0002209]
Sparse, thin scalp hair [HPO:0002209]
sparse-absent scalp hair [HPO:0002209]
Thin scalp hair [HPO:0002209]
Decreased scalp hair [Orphanet:24080]
Sparse scalp hair [OMIM:Sparse scalp hair]
Sparse, thin scalp hair [OMIM:Sparse, thin scalp hair]
Sparse-absent scalp hair [OMIM:Sparse-absent scalp hair]
Thin scalp hair [OMIM:Thin scalp hair]
Hypotrichosis/atrichia/atrichiasis/scalp hairlessness [Orphanet:24080]
Sparse scalp hair (classic feature) [OMIM:Sparse scalp hair (classic feature)]
Sparse scalp hair (in some patients) [OMIM:Sparse scalp hair (in some patients)]
Quality:
Cross references:
Orphanet:24080 "Hypotrichosis/atrichia/atrichiasis/scalp hairlessness" [Orphanet:24080]
OMIM: "Sparse scalp hair" [OMIM:Sparse scalp hair]
OMIM: "Sparse, thin scalp hair" [OMIM:Sparse, thin scalp hair]
OMIM: "Sparse-absent scalp hair" [OMIM:Sparse-absent scalp hair]
OMIM: "Thin scalp hair" [OMIM:Thin scalp hair]
OMIM: "Sparse scalp hair (classic feature)" [OMIM:Sparse scalp hair (classic feature)]
OMIM: "Sparse scalp hair (in some patients)" [OMIM:Sparse scalp hair (in some patients)]
Is a (Direct Parents):
Orphanet Abnormality of the hair
HPO         Abnormality of the scalp hair
Orphanet Hypotrichosis
HPO         Sparse hair
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the scalp(HPO:0001965)
                Abnormality of the scalp hair(HPO:0100037)
                   Sparse scalp hair(HPO:0002209)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormality of the scalp hair(HPO:0100037)
                   Sparse scalp hair(HPO:0002209)
                Abnormality of hair density(HPO:0011357)
                   Sparse hair(HPO:0008070)
                      Sparse scalp hair(HPO:0002209)
MedDRA:
Database Frequency: 59 / 7739
Resource:

All diseases associated with this symptom:

ADULT syndrome (Orphanet:978)
AREDYLD syndrome (Orphanet:1133)
Argininosuccinic aciduria (Orphanet:23)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Classical phenylketonuria (Orphanet:79254)
Coffin-Siris syndrome (Orphanet:1465)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
DWARFISM, FAMILIAL, WITH MUSCLE SPASMS (OMIM:600771)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 1 (OMIM:224230)
Dubowitz syndrome (Orphanet:235)
ECTODERMAL DYSPLASIA 5, HAIR/NAIL TYPE (OMIM:614927)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
Ectodermal dysplasia with natal teeth, Turnpenny type (Orphanet:69083)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Fried's tooth and nail syndrome (Orphanet:99672)
Genitopatellar syndrome (Orphanet:85201)
HYPOTRICHOSIS 8 (OMIM:278150)
Hawkinsinuria (Orphanet:2118)
Hereditary hypotrichosis with recurrent skin vesicles (Orphanet:217407)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis simplex (Orphanet:55654)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Johanson-Blizzard syndrome (Orphanet:2315)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Langer-Giedion syndrome (Orphanet:502)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 (OMIM:614607)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 (OMIM:614609)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Mandibuloacral dysplasia (Orphanet:2457)
Menkes disease (Orphanet:565)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Netherton syndrome (Orphanet:634)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Oligodontia - cancer predisposition syndrome (Orphanet:300576)
PACHYONYCHIA CONGENITA 2 (OMIM:167210)
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR (OMIM:616099)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Steinert myotonic dystrophy (Orphanet:273)
Transaldolase deficiency (Orphanet:101028)
Trichodysplasia - xeroderma (Orphanet:3361)
Werner syndrome (Orphanet:902)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wilson-Turner syndrome (Orphanet:3459)
Woodhouse-Sakati syndrome (Orphanet:3464)
Yunis-Varon syndrome (Orphanet:3472)