Abnormality of the hairline

Symptom Information:

Symptom ID: HPO:0009553
Synonyms:
Abnormal hairline position [Orphanet:24760]
Abnormal implantation of hair [Orphanet:24760]
Quality:
Cross references:
Orphanet:24760 "Abnormal implantation of hair" [Orphanet:24760]
Is a (Direct Parents):
HPO         Congenital abnormal hair pattern
HPO         Abnormality of the scalp hair
Orphanet Abnormality of the hair
HPO         Abnormality of the posterior hairline
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 the scalp hair(HPO:0100037)
                   Abnormality of the hairline(HPO:0009553)
                Abnormal hair pattern(HPO:0010720)
                   Congenital abnormal hair pattern(HPO:0011361)
                      Abnormality of the hairline(HPO:0009553)
       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)
                   Abnormality of the hairline(HPO:0009553)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

16q24.3 microdeletion syndrome (Orphanet:261250)
1p36 deletion syndrome (Orphanet:1606)
8q22.1 microdeletion syndrome (Orphanet:178303)
Ablepharon macrostomia syndrome (Orphanet:920)
Acrofacial dysostosis, Catania type (Orphanet:1786)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Braddock syndrome (Orphanet:52047)
C syndrome (Orphanet:1308)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Disorder of sex development - intellectual deficit (Orphanet:2983)
Distal trisomy 18q (Orphanet:1716)
Facial ectodermal dysplasia (Orphanet:1807)
Fraser syndrome (Orphanet:2052)
Gonadal dysgenesis, XY type - associated anomalies (Orphanet:1770)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Intellectual deficit, X-linked, Vitale type (Orphanet:85289)
Johanson-Blizzard syndrome (Orphanet:2315)
Marden-Walker syndrome (Orphanet:2461)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Oculotrichoanal syndrome (Orphanet:2717)
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) (OMIM:614886)
Pachydermoperiostosis (Orphanet:2796)
Prader-Willi syndrome (Orphanet:739)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Ring chromosome 1 (Orphanet:1437)
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion (Orphanet:353281)
SCARF syndrome (Orphanet:3134)
Trisomy 4p (Orphanet:1738)