Abnormality of the hair
Symptom Information:
| Symptom ID: | HPO:0001595 | ||||
| Synonyms: |
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| Cross references: |
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| 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) MedDRA: |
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| Database Frequency: | 89 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 2q31.1 microdeletion syndrome | (Orphanet:251014) |
| 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency | (Orphanet:753) |
| ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS | (OMIM:601427) |
| Acquired epidermolysis bullosa | (Orphanet:46487) |
| Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
| Amelo-onycho-hypohidrotic syndrome | (Orphanet:1028) |
| Ataxia-telangiectasia | (Orphanet:100) |
| Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
| Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
| Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
| Birt-Hogg-Dube syndrome | (Orphanet:122) |
| Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
| Braddock syndrome | (Orphanet:52047) |
| Brittle cornea syndrome | (Orphanet:90354) |
| CATATRICHY | (OMIM:116850) |
| Cockayne syndrome | (Orphanet:191) |
| Congenital hypothyroidism | (Orphanet:442) |
| Congenital hypothyroidism due to developmental anomaly | (Orphanet:95711) |
| Costello syndrome | (Orphanet:3071) |
| DISCOID FIBROMAS, FAMILIAL MULTIPLE | (OMIM:190340) |
| Darier disease | (Orphanet:218) |
| Dermo-odonto dysplasia | (Orphanet:1660) |
| Dissecting cellulitis of the scalp | (Orphanet:345) |
| EYEBROW, WHORL IN | (OMIM:133800) |
| Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
| Ellis Van Creveld syndrome | (Orphanet:289) |
| Erosive pustular dermatosis of the scalp | (Orphanet:222) |
| Erythrokeratodermia variabilis | (Orphanet:317) |
| Familial melanoma | (Orphanet:618) |
| GRANDDAD SYNDROME | (OMIM:138920) |
| HAIR WHORL | (OMIM:139400) |
| HAIRY NOSE TIP | (OMIM:139630) |
| Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
| Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
| Hidrotic ectodermal dysplasia, Christianson-Fourie type | (Orphanet:1808) |
| ICHTHYOSIS, SPLIT HAIRS, AND AMINO ACIDURIA | (OMIM:242550) |
| Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
| Incontinentia pigmenti | (Orphanet:464) |
| Inherited epidermolysis bullosa | (Orphanet:79361) |
| Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
| Intestinal lymphangiectasia | (Orphanet:36204) |
| Juvenile hyaline fibromatosis | (Orphanet:2028) |
| Keratosis palmoplantaris striata | (Orphanet:50942) |
| Knobloch syndrome | (Orphanet:1571) |
| Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
| Loose anagen syndrome | (Orphanet:168) |
| METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
| MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES | (OMIM:607597) |
| MIDPHALANGEAL HAIR | (OMIM:157200) |
| Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
| Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
| Microphthalmia with limb anomalies | (Orphanet:1106) |
| Multiple carboxylase deficiency | (Orphanet:148) |
| Netherton syndrome | (Orphanet:634) |
| Neu-Laxova syndrome | (Orphanet:2671) |
| Nevus comedonicus syndrome | (Orphanet:64754) |
| Nijmegen breakage syndrome | (Orphanet:647) |
| OCCIPITAL HAIR, WHITE LOCK OF | (OMIM:310900) |
| Oculocutaneous albinism type 3 | (Orphanet:79433) |
| Oculocutaneous albinism type 6 | (Orphanet:370097) |
| Oculoosteocutaneous syndrome | (Orphanet:2713) |
| Oculotrichoanal syndrome | (Orphanet:2717) |
| PREMATURE AGING SYNDROME, OKAMOTO TYPE | (OMIM:601811) |
| Pachyonychia congenita | (Orphanet:2309) |
| Pili bifurcati | (Orphanet:720) |
| Pili gemini | (Orphanet:79492) |
| Primary cutaneous lymphoma | (Orphanet:542) |
| Progeroid syndrome, Petty type | (Orphanet:2963) |
| Pseudo-pelade of Brocq | (Orphanet:129) |
| Quinquaud's folliculitis decalvans | (Orphanet:346) |
| RED SKIN PIGMENT ANOMALY OF NEW GUINEA | (OMIM:266350) |
| Recessive dystrophic epidermolysis bullosa-generalized other | (Orphanet:89842) |
| Recombinant 8 syndrome | (Orphanet:96167) |
| Ringed hair disease | (Orphanet:169) |
| Rothmund-Thomson syndrome | (Orphanet:2909) |
| SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 6 | (OMIM:210750) |
| Satoyoshi syndrome | (Orphanet:3130) |
| Self-healing collodion baby | (Orphanet:281122) |
| TENTED EYEBROWS | (OMIM:611426) |
| Testotoxicosis | (Orphanet:3000) |
| Thrombocytopenia - Robin sequence | (Orphanet:3323) |
| Treacher-Collins syndrome | (Orphanet:861) |
| Tricho-dento-osseous syndrome | (Orphanet:3352) |
| Uncombable hair syndrome | (Orphanet:1410) |
| VAN BOGAERT-HOZAY SYNDROME | (OMIM:277150) |
| Waardenburg syndrome type 1 | (Orphanet:894) |
| Werner syndrome | (Orphanet:902) |
| Woolly hair - hypotrichosis - everted lower lip - outstanding ears | (Orphanet:1409) |
| Wrinkly skin syndrome | (Orphanet:2834) |