Widow's peak

Symptom Information:

Symptom ID: HPO:0000349
Synonyms:
Widow's peak [OMIM:Widow's peak]
High hair line (front)/widow peak [Orphanet:24840]
Quality:
Cross references:
Orphanet:24840 "High hair line (front)/widow peak" [Orphanet:24840]
OMIM: "Widow's peak" [OMIM:Widow's peak]
Is a (Direct Parents):
HPO         High anterior hairline
Orphanet Abnormality of the 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)
                Abnormal hair pattern(HPO:0010720)
                   Congenital abnormal hair pattern(HPO:0011361)
                      Abnormality of the hairline(HPO:0009553)
                         Abnormality of the frontal hairline(HPO:0000599)
                            High anterior hairline(HPO:0009890)
                               Widow's peak(HPO:0000349)
                Abnormality of the scalp hair(HPO:0100037)
                   Abnormality of the hairline(HPO:0009553)
                      Abnormality of the frontal hairline(HPO:0000599)
                         High anterior hairline(HPO:0009890)
                            Widow's peak(HPO:0000349)
       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)
                      Abnormality of the frontal hairline(HPO:0000599)
                         High anterior hairline(HPO:0009890)
                            Widow's peak(HPO:0000349)
             Abnormality of the face(HPO:0000271)
                Abnormality of the forehead(HPO:0000290)
                   Abnormality of the frontal hairline(HPO:0000599)
                      High anterior hairline(HPO:0009890)
                         Widow's peak(HPO:0000349)
MedDRA:
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
Aarskog-Scott syndrome (Orphanet:915)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Craniofrontonasal dysplasia (Orphanet:1520)
Cyprus facial-neuromusculoskeletal syndrome (Orphanet:2674)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Donnai-Barrow syndrome (Orphanet:2143)
Frontonasal dysplasia (Orphanet:250)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypertelorism, Teebi type (Orphanet:1519)
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM (OMIM:606242)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Opitz G/BBB syndrome (Orphanet:2745)
Schilbach-Rott syndrome (Orphanet:2353)
Trisomy 17p (Orphanet:261290)
WIDOW'S PEAK (OMIM:194000)
WIDOW'S PEAK SYNDROME (OMIM:314570)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked Opitz G/BBB syndrome (Orphanet:306597)