Depressed nasal tip

Symptom Information:

Symptom ID: HPO:0000437
Synonyms:
Flat nasal tip [HPO:0000437]
Flattened nasal tip [HPO:0000437]
Nasal tip, depressed [HPO:0000437]
Nasal tip, recessed [HPO:0000437]
Nasal tip, retruded [HPO:0000437]
Depressed nasal tip [OMIM:Depressed nasal tip]
Flat nasal tip [OMIM:Flat nasal tip]
Flattened nasal tip [OMIM:Flattened nasal tip]
Short columella/depressed nasal tip [Orphanet:8570]
Quality:
Cross references:
HPO:0011833 "Overhanging nasal tip" [Orphanet:8570]
Orphanet:8570 "Short columella/depressed nasal tip" [Orphanet:8570]
OMIM: "Depressed nasal tip" [OMIM:Depressed nasal tip]
OMIM: "Flat nasal tip" [OMIM:Flat nasal tip]
OMIM: "Flattened nasal tip" [OMIM:Flattened nasal tip]
Is a (Direct Parents):
Orphanet Abnormality of the nose
HPO         Abnormality of the nasal tip
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormality of the external nose(HPO:0010938)
                      Abnormality of the nasal tip(HPO:0000436)
                         Depressed nasal tip(HPO:0000437)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

3MC SYNDROME 2 (OMIM:265050)
AREDYLD syndrome (Orphanet:1133)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
FEINGOLD SYNDROME 1 (OMIM:164280)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Feingold syndrome (Orphanet:1305)
Fetal akinesia deformation sequence (Orphanet:994)
HOLOPROSENCEPHALY 4 (OMIM:142946)
HOLOPROSENCEPHALY 7 (OMIM:610828)
Hypoplastic tibiae - postaxial polydactyly (Orphanet:3332)
KABUKI SYNDROME 1 (OMIM:147920)
KABUKI SYNDROME 2 (OMIM:300867)
Kabuki syndrome (Orphanet:2322)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)