Sparse hair

Symptom Information:

Symptom ID: HPO:0008070
Synonyms:
Thin hair [HPO:0008070]
THIN, SPARSE HAIR [HPO:0008070]
Thinned hair [HPO:0008070]
Sparse hair [OMIM:Sparse hair]
Thin hair [OMIM:Thin hair]
Thin, sparse hair [OMIM:Thin, sparse hair]
Sparse hair (1 patient) [OMIM:Sparse hair (1 patient)]
Sparse hair (in 1 family) [OMIM:Sparse hair (in 1 family)]
Sparse hair (in some patients) [OMIM:Sparse hair (in some patients)]
Sparse hair (infancy) [OMIM:Sparse hair (infancy)]
Sparse, thin hair [OMIM:Sparse, thin hair]
Thin hair (in some patients) [OMIM:Thin hair (in some patients)]
Thin, sparse hair (childhood) [OMIM:Thin, sparse hair (childhood)]
Quality:
Cross references:
OMIM: "Sparse hair" [OMIM:Sparse hair]
OMIM: "Thin hair" [OMIM:Thin hair]
OMIM: "Thin, sparse hair" [OMIM:Thin, sparse hair]
OMIM: "Sparse hair (1 patient)" [OMIM:Sparse hair (1 patient)]
OMIM: "Sparse hair (in 1 family)" [OMIM:Sparse hair (in 1 family)]
OMIM: "Sparse hair (in some patients)" [OMIM:Sparse hair (in some patients)]
OMIM: "Sparse hair (infancy)" [OMIM:Sparse hair (infancy)]
OMIM: "Sparse, thin hair" [OMIM:Sparse, thin hair]
OMIM: "Thin hair (in some patients)" [OMIM:Thin hair (in some patients)]
OMIM: "Thin, sparse hair (childhood)" [OMIM:Thin, sparse hair (childhood)]
Is a (Direct Parents):
HPO         Abnormality of hair density
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 density(HPO:0011357)
                   Sparse hair(HPO:0008070)
MedDRA:
Database Frequency: 94 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2q32q33 microdeletion syndrome (Orphanet:251019)
5p13 microduplication syndrome (Orphanet:329802)
8q22.1 microdeletion syndrome (Orphanet:178303)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
ANGIOMA SERPIGINOSUM, X-LINKED (OMIM:300652)
AREDYLD syndrome (Orphanet:1133)
Acro-osteolysis-keloid-like lesions-premature aging syndrome (Orphanet:363665)
Alström syndrome (Orphanet:64)
Autosomal dominant chondrodysplasia punctata (Orphanet:79344)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
COCKAYNE SYNDROME A (OMIM:216400)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Coats plus syndrome (Orphanet:313838)
Cockayne syndrome (Orphanet:191)
Costello syndrome (Orphanet:3071)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Craniolenticulosutural dysplasia (Orphanet:50814)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
De Barsy syndrome (Orphanet:2962)
Dyskeratosis congenita (Orphanet:1775)
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT (OMIM:614940)
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:614941)
ECTODERMAL DYSPLASIA, ANHIDROTIC, WITH T-CELL IMMUNODEFICIENCY, AUTOSOMALDOMINANT (OMIM:612132)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2 (OMIM:615349)
Ectodermal dysplasia - blindness (Orphanet:1806)
Filippi syndrome (Orphanet:3255)
Focal dermal hypoplasia (Orphanet:2092)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Hallermann-Streiff syndrome (Orphanet:2108)
Hypodontia - dysplasia of nails (Orphanet:2228)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Kaler-Garrity-Stern syndrome (Orphanet:2324)
Lenz-Majewski hyperostotic dwarfism (Orphanet:2658)
Loose anagen syndrome (Orphanet:168)
Lysinuric protein intolerance (Orphanet:470)
MACS syndrome (Orphanet:217335)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 15 (OMIM:614608)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 18 (OMIM:615074)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM (OMIM:606242)
MGAT2-CDG (Orphanet:79329)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
McDonough syndrome (Orphanet:2471)
Menkes disease (Orphanet:565)
Moynahan syndrome (Orphanet:2574)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Myhre syndrome (Orphanet:2588)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
ONYCHOGRYPOSIS, PEDAL, WITH KERATOSIS PLANTARIS AND COARSE HAIR (OMIM:164680)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculodentodigital dysplasia (Orphanet:2710)
Oculoosteocutaneous syndrome (Orphanet:2713)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
RAPP-HODGKIN SYNDROME (OMIM:129400)
ROBERTS SYNDROME (OMIM:268300)
Renpenning syndrome (Orphanet:3242)
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism (Orphanet:3085)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Roberts syndrome (Orphanet:3103)
Rothmund-Thomson syndrome (Orphanet:2909)
SC PHOCOMELIA SYNDROME (OMIM:269000)
SCARF syndrome (Orphanet:3134)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Scalp-ear-nipple syndrome (Orphanet:2036)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)
Syndromic diarrhea (Orphanet:84064)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
TRICHOHEPATOENTERIC SYNDROME 2 (OMIM:614602)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 (OMIM:234050)
Taurodontia - absent teeth - sparse hair (Orphanet:2731)
Trichodental syndrome (Orphanet:3351)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Weaver syndrome (Orphanet:3447)
Woodhouse-Sakati syndrome (Orphanet:3464)
Wrinkly skin syndrome (Orphanet:2834)
Zunich-Kaye syndrome (Orphanet:3474)