modern wellness · Symptom
Abnormal foot morphology
🩺 HPO Source
HPO ID
HPO Label
Abnormal foot morphology
HPO Definition
An abnormality of the skeleton of foot.
HPO Curator Comment
A disorder of the foot that can either be congenital or acquired. Such deformities can include hammer toe, club foot deformity, flat feet, pes cavus, congenital vertical talus (rocker bottom foot), and many others.
🔤 Synonyms (5)
Synonyms
Abnormal feet structureAbnormality of the feetAbnormality of the footFoot deformitiesFoot deformity
🔗 Cross-References (2)
SNOMEDCT_US229844004
UMLSC0016506
🔼 Broader Terms (1)
HP:0002814Abnormality of the lower limb
🏥 Conditions where Abnormal foot morphology appears
32 · bridged via HPO ↔ OMIM
disease OMIM 200610
Achondrogenesis Type 2
ev: IEA
syndrome OMIM 146300
Adult Hypophosphatasia (Disorder)
ev: IEA
syndrome OMIM 617822
Alkuraya-Kucinskas Syndrome
ev: IEA
syndrome OMIM 618218
Baker-Gordon Syndrome
ev: IEA
syndrome OMIM 249620
Blepharophimosis Syndrome Ohdo Type
ev: IEA
syndrome OMIM 616849
Brachydactyly, Type A1, D
freq: 0/2 ev: PCS
syndrome OMIM 608836
Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal
ev: IEA
syndrome OMIM 608323
Charcot-Marie-Tooth Disease, Dominant Intermediate C
ev: IEA
syndrome OMIM 263750
Genee-Wiedemann Syndrome
ev: IEA
syndrome OMIM 129500
Hidrotic Ectodermal Dysplasia
ev: IEA
disease OMIM 200610
Hypochondrogenesis
ev: IEA
syndrome OMIM 601553
Hypotrichosis, Congenital, With Juvenile Macular Dystrophy
freq: 0/1 ev: PCS
syndrome OMIM 269920
Infantile Sialic Acid Storage Disease
ev: IEA
syndrome OMIM 137200
Isaacs Syndrome
ev: TAS
syndrome OMIM 608091
Joubert Syndrome 2
ev: IEA
syndrome OMIM 615599
Mental Retardation, Autosomal Recessive 40
freq: 2/2 ev: PCS
syndrome OMIM 300243
Mental Retardation, X-Linked, Syndromic, Christianson Type
ev: IEA
syndrome OMIM 300868
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2
freq: 1/1 ev: PCS
syndrome OMIM 618198
Myasthenic Syndrome, Congenital, 24, Presynaptic
ev: IEA
syndrome OMIM 269920
N-Acetylneuraminic Acid Storage Disease
ev: IEA
syndrome OMIM 618186
Neuropathy, Congenital Hypomyelinating, 3
ev: IEA
syndrome OMIM 256840
Neuropathy, Hereditary Sensory, With Spastic Paraplegia, Autosomal Recessive
ev: PCS
syndrome OMIM 614369
Peripheral Neuropathy, Myopathy, Hoarseness, And Hearing Loss
freq: 10/15 ev: PCS
syndrome OMIM 221770
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1
ev: IEA
syndrome OMIM 607596
Pontocerebellar Hypoplasia Type 1
ev: IEA
syndrome OMIM 614678
Pontocerebellar Hypoplasia, Type 1B
ev: TAS
disease OMIM 208230
Progressive Pseudorheumatoid Dysplasia
ev: IEA
syndrome OMIM 618205
Snijders Blok-Campeau Syndrome
ev: IEA
syndrome OMIM 158600
Spinal Muscular Atrophy, Childhood, Proximal, Autosomal Dominant
ev: TAS
disease OMIM 184252
Spondylometaphyseal Dysplasia, Kozlowski Type
ev: IEA
syndrome OMIM 601390
Van Maldergem Syndrome 1
ev: TAS
syndrome OMIM 601390
Van Maldergem Wetzburger Verloes Syndrome
ev: TAS