Abnormal hair quantity

Symptom Information:

Symptom ID: HPO:0011362
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the hair
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of skin adnexa(HPO:0011138)
             Abnormality of the hair(HPO:0001595)
                Abnormal hair quantity(HPO:0011362)
Database Frequency: 92 / 7739

All diseases associated with this symptom:

17q21.31 microduplication syndrome (Orphanet:217340)
19p13.12 microdeletion syndrome (Orphanet:254346)
1p36 deletion syndrome (Orphanet:1606)
2q23.1 microdeletion syndrome (Orphanet:228402)
4q21 microdeletion syndrome (Orphanet:238750)
ACTH-dependent Cushing syndrome (Orphanet:99892)
ACTH-independent Cushing syndrome (Orphanet:99893)
ACTH-independent macronodular adrenal hyperplasia (Orphanet:189427)
AREDYLD syndrome (Orphanet:1133)
Acanthosis nigricans (Orphanet:924)
Acquired hypertrichosis lanuginosa (Orphanet:2221)
Acromegaly (Orphanet:963)
Acroosteolysis, dominant type (Orphanet:955)
Argininosuccinic aciduria (Orphanet:23)
Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)
Barber-Say syndrome (Orphanet:1231)
Bohring-Opitz syndrome (Orphanet:97297)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Castleman disease (Orphanet:160)
Cataract - deafness - hypogonadism (Orphanet:1383)
Cataract - hypertrichosis - intellectual deficit (Orphanet:1375)
Cervical hypertrichosis - peripheral neuropathy (Orphanet:2218)
Classical phenylketonuria (Orphanet:79254)
Coffin-Siris syndrome (Orphanet:1465)
Congenital erythropoietic porphyria (Orphanet:79277)
Cornelia de Lange syndrome (Orphanet:199)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Curry-Jones syndrome (Orphanet:1553)
Cushing syndrome due to ectopic ACTH secretion (Orphanet:99889)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Diastematomyelia (Orphanet:1671)
Dwarfism - intellectual deficit - eye abnormality (Orphanet:2650)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
Edinburgh malformation syndrome (Orphanet:1895)
Epilepsy - microcephaly - skeletal dysplasia (Orphanet:1948)
Erythrokeratodermia variabilis (Orphanet:317)
Fetal alcohol syndrome (Orphanet:1915)
Fetal minoxidil syndrome (Orphanet:1918)
Floating-Harbor syndrome (Orphanet:2044)
GM1 gangliosidosis (Orphanet:354)
Gingival fibromatosis-hypertrichosis syndrome (Orphanet:2026)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Grix-Blankenship-Peterson syndrome (Orphanet:2099)
Hawkinsinuria (Orphanet:2118)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertrichosis (Orphanet:79365)
Hypertrichosis cubiti - short stature (Orphanet:2220)
Hypertrichosis lanuginosa congenita (Orphanet:2222)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration (Orphanet:85317)
Ito hypomelanosis (Orphanet:435)
Large congenital melanocytic nevus (Orphanet:626)
Lowry-MacLean syndrome (Orphanet:2409)
Mal de Meleda (Orphanet:87503)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Marshall-Smith syndrome (Orphanet:561)
Menkes disease (Orphanet:565)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Micro syndrome (Orphanet:2510)
Microlissencephaly - micromelia (Orphanet:50810)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria (Orphanet:1933)
Mucolipidosis type 2 (Orphanet:576)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 3 (Orphanet:581)
Multiple benign circumferential skin creases on limbs (Orphanet:2505)
Neurocutaneous melanocytosis (Orphanet:2481)
Okamoto syndrome (Orphanet:2729)
POEMS syndrome (Orphanet:2905)
Papillon-Lefèvre syndrome (Orphanet:678)
Parana hard-skin syndrome (Orphanet:2812)
Porphyria cutanea tarda (Orphanet:101330)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Progeroid syndrome, Petty type (Orphanet:2963)
Prolidase deficiency (Orphanet:742)
Proteus syndrome (Orphanet:744)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Ramon syndrome (Orphanet:3019)
Rubinstein-Taybi syndrome (Orphanet:783)
Ruvalcaba syndrome (Orphanet:3121)
Schinzel-Giedion syndrome (Orphanet:798)
Schwartz-Jampel syndrome (Orphanet:800)
Sinus node disease and myopia (OMIM:182190)
Steinert myotonic dystrophy (Orphanet:273)
Torg-Winchester syndrome (Orphanet:3460)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trisomy 17p (Orphanet:261290)
Werner syndrome (Orphanet:902)
Zimmermann-Laband syndrome (Orphanet:3473)