Human Phenotype Ontology 
Grandparent Node:
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Abnormal hard palate morphology (HP:0100737)help
Grandparent Node:
expand
Oral cleft (HP:0000202)help
Parent Node:
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Cleft palate (HP:0000175)help
..Starting node
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Submucous cleft of soft and hard palate (HP:0410031)help
Term ID: 410031
Name: Submucous cleft of soft and hard palate
Synonym:
Definition: Soft and hard-palate submucous clefts are characterized by bony defects in the midline of the soft and hard palate that are covered by the lining (ie mucous membrane) of the roof of the mouth.
Comments:
Reference: HP:0410031
Genes and Diseases:
 
       Child Nodes:
........expandSubmucous cleft hard palate (HP:0000176) help

 Sister Nodes: 
..expandCleft maxillary alveolus (HP:0410003) help
..expandMedian cleft palate (HP:0009099) help
..expandNon-midline cleft palate (HP:0100338) help
..expandobsolete Cleft secondary palate (HP:0410004) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410031HP:0410031Submucous cleft of soft and hard palate0AMER1 CL E G H13928526837ORPHA:2780Osteopathia striata-cranial sclerosis syndrome34
HP:0410031HP:0410031Submucous cleft of soft and hard palate0AMMECR1 CL E G H9949467OMIM:300990Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis2
HP:0410031HP:0410031Submucous cleft of soft and hard palate0B3GALNT2 CL E G H14878928596ORPHA:899Walker-Warburg syndrome43
HP:0410031HP:0410031Submucous cleft of soft and hard palate0B4GAT1 CL E G H1104115685ORPHA:899Walker-Warburg syndrome17
HP:0410031HP:0410031Submucous cleft of soft and hard palate0BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2101
HP:0410031HP:0410031Submucous cleft of soft and hard palate0BCOR CL E G H5488020893ORPHA:2712Oculofaciocardiodental syndrome101
HP:0410031HP:0410031Submucous cleft of soft and hard palate0BICRA CL E G H299984332OMIM:619325COFFIN-SIRIS SYNDROME 12; CSS122
HP:0410031HP:0410031Submucous cleft of soft and hard palate0BRAF CL E G H6731097ORPHA:1340Cardiofaciocutaneous syndrome276
HP:0410031HP:0410031Submucous cleft of soft and hard palate0BRAF CL E G H6731097OMIM:115150Cardiofaciocutaneous syndrome 1276
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CARS1 CL E G H8331493OMIM:618891MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME; MDBH
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CDC45 CL E G H83181739ORPHA:2554Ear-patella-short stature syndrome9
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CDC6 CL E G H9901744ORPHA:2554Ear-patella-short stature syndrome31
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CDC6 CL E G H9901744OMIM:613805Meier-Gorlin syndrome 531
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CDH11 CL E G H10091750ORPHA:1299Branchioskeletogenital syndrome2
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CDT1 CL E G H8162024576ORPHA:2554Ear-patella-short stature syndrome50
HP:0410031HP:0410031Submucous cleft of soft and hard palate0COL2A1 CL E G H12802200OMIM:108300Stickler syndrome, type I284
HP:0410031HP:0410031Submucous cleft of soft and hard palate0COL4A1 CL E G H12822202ORPHA:899Walker-Warburg syndrome193
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CRPPA CL E G H72992037276ORPHA:899Walker-Warburg syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0CUL3 CL E G H84522553OMIM:619239NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES; NEDAUS92
HP:0410031HP:0410031Submucous cleft of soft and hard palate0DAG1 CL E G H16052666ORPHA:899Walker-Warburg syndrome108
HP:0410031HP:0410031Submucous cleft of soft and hard palate0DGCR2 CL E G H99932845OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0DGCR6 CL E G H82142846OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0DGCR8 CL E G H544872847OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0DHCR24 CL E G H17182859ORPHA:35107Desmosterolosis72
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ESS2 CL E G H822016817OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0FKRP CL E G H7914717997ORPHA:899Walker-Warburg syndrome157
HP:0410031HP:0410031Submucous cleft of soft and hard palate0FKTN CL E G H22183622ORPHA:899Walker-Warburg syndrome184
HP:0410031HP:0410031Submucous cleft of soft and hard palate0FOXP2 CL E G H9398613875ORPHA:209908Childhood apraxia of speech143
HP:0410031HP:0410031Submucous cleft of soft and hard palate0GDF11 CL E G H102204216OMIM:619122VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES; VHO
HP:0410031HP:0410031Submucous cleft of soft and hard palate0GMNN CL E G H5105317493ORPHA:2554Ear-patella-short stature syndrome3
HP:0410031HP:0410031Submucous cleft of soft and hard palate0HAAO CL E G H234984796OMIM:617660Vertebral, cardiac, renal, and limb defects syndrome 12
HP:0410031HP:0410031Submucous cleft of soft and hard palate0HS2ST1 CL E G H96535193OMIM:619194NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS; NFSRA
HP:0410031HP:0410031Submucous cleft of soft and hard palate0HYAL1 CL E G H33735320OMIM:601492Mucopolysaccharidosis type IX28
HP:0410031HP:0410031Submucous cleft of soft and hard palate0HYLS1 CL E G H21984426558ORPHA:2189Hydrolethalus31
HP:0410031HP:0410031Submucous cleft of soft and hard palate0KAT5 CL E G H105245275OMIM:619103NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB1
HP:0410031HP:0410031Submucous cleft of soft and hard palate0KAT6B CL E G H2352217582ORPHA:3047Blepharophimosis-intellectual disability syndrome, SBBYS type141
HP:0410031HP:0410031Submucous cleft of soft and hard palate0KIF7 CL E G H37465430497ORPHA:2189Hydrolethalus167
HP:0410031HP:0410031Submucous cleft of soft and hard palate0KRAS CL E G H38456407ORPHA:1340Cardiofaciocutaneous syndrome196
HP:0410031HP:0410031Submucous cleft of soft and hard palate0LARGE1 CL E G H92156511ORPHA:899Walker-Warburg syndrome136
HP:0410031HP:0410031Submucous cleft of soft and hard palate0LIG4 CL E G H39816601ORPHA:235Dubowitz syndrome88
HP:0410031HP:0410031Submucous cleft of soft and hard palate0LMNA CL E G H40006636ORPHA:1662Restrictive dermopathy645
HP:0410031HP:0410031Submucous cleft of soft and hard palate0MAP2K1 CL E G H56046840ORPHA:1340Cardiofaciocutaneous syndrome134
HP:0410031HP:0410031Submucous cleft of soft and hard palate0MAP2K2 CL E G H56056842ORPHA:1340Cardiofaciocutaneous syndrome178
HP:0410031HP:0410031Submucous cleft of soft and hard palate0NSUN2 CL E G H5488825994ORPHA:235Dubowitz syndrome84
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ORC1 CL E G H49988487ORPHA:2554Ear-patella-short stature syndrome53
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ORC4 CL E G H50008490ORPHA:2554Ear-patella-short stature syndrome21
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ORC6 CL E G H2359417151ORPHA:2554Ear-patella-short stature syndrome39
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PIEZO2 CL E G H6389526270OMIM:114300Arthrogryposis, distal, type 377
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PIEZO2 CL E G H6389526270ORPHA:2461Marden-Walker syndrome77
HP:0410031HP:0410031Submucous cleft of soft and hard palate0POMGNT1 CL E G H5562419139ORPHA:899Walker-Warburg syndrome180
HP:0410031HP:0410031Submucous cleft of soft and hard palate0POMGNT2 CL E G H8489225902ORPHA:899Walker-Warburg syndrome33
HP:0410031HP:0410031Submucous cleft of soft and hard palate0POMK CL E G H8419726267ORPHA:899Walker-Warburg syndrome18
HP:0410031HP:0410031Submucous cleft of soft and hard palate0POMT1 CL E G H105859202ORPHA:899Walker-Warburg syndrome213
HP:0410031HP:0410031Submucous cleft of soft and hard palate0POMT2 CL E G H2995419743ORPHA:899Walker-Warburg syndrome221
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PPP2R5D CL E G H55289312ORPHA:457279Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome10
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PRKAR1B CL E G H55759390OMIM:619680MARBACH-SCHAAF NEURODEVELOPMENTAL SYNDROME; MASNS2
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PRR12 CL E G H5747929217OMIM:619539NEUROOCULAR SYNDROME; NOC1
HP:0410031HP:0410031Submucous cleft of soft and hard palate0PTDSS1 CL E G H97919587ORPHA:2658Lenz-Majewski hyperostotic dwarfism6
HP:0410031HP:0410031Submucous cleft of soft and hard palate0RAD21 CL E G H58859811OMIM:614701Cornelia de Lange syndrome 425
HP:0410031HP:0410031Submucous cleft of soft and hard palate0RNU4ATAC CL E G H10015168334016ORPHA:2636Microcephalic osteodysplastic primordial dwarfism types I and III15
HP:0410031HP:0410031Submucous cleft of soft and hard palate0RPS23 CL E G H622810410OMIM:617412BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD2
HP:0410031HP:0410031Submucous cleft of soft and hard palate0RXYLT1 CL E G H1032913530ORPHA:899Walker-Warburg syndrome
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SET CL E G H641810760OMIM:618106Mental retardation, autosomal dominant 581
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SIAH1 CL E G H647710857OMIM:619314BURATTI-HAREL SYNDROME; BURHAS
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SIX3 CL E G H649610889OMIM:157170Holoprosencephaly 232
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SMAD4 CL E G H40896770ORPHA:2588Myhre syndrome504
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SMCHD1 CL E G H2334729090ORPHA:2250Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome174
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SON CL E G H665111183OMIM:617140Zttk syndrome12
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SOX6 CL E G H5555316421OMIM:618971TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS1
HP:0410031HP:0410031Submucous cleft of soft and hard palate0SOX9 CL E G H666211204OMIM:114290Campomelic dysplasia109
HP:0410031HP:0410031Submucous cleft of soft and hard palate0STAG2 CL E G H1073511355OMIM:301043HOLOPROSENCEPHALY 13, X-LINKED; HPE131
HP:0410031HP:0410031Submucous cleft of soft and hard palate0TBX1 CL E G H689911592OMIM:192430Velocardiofacial syndrome32
HP:0410031HP:0410031Submucous cleft of soft and hard palate0TCTN3 CL E G H2612324519ORPHA:2753Orofaciodigital syndrome type 431
HP:0410031HP:0410031Submucous cleft of soft and hard palate0WBP11 CL E G H5172916461OMIM:619227VERTEBRAL, CARDIAC, TRACHEOESOPHAGEAL, RENAL, AND LIMB DEFECTS; VCTERL
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ZEB2 CL E G H983914881OMIM:235730Mowat-Wilson syndrome362
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ZEB2 CL E G H983914881ORPHA:261552Mowat-Wilson syndrome due to a ZEB2 point mutationHP:0040284 - Very rare362
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ZEB2 CL E G H983914881ORPHA:261537Mowat-Wilson syndrome due to monosomy 2q22HP:0040284 - Very rare362
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ZMPSTE24 CL E G H1026912877ORPHA:1662Restrictive dermopathy83
HP:0410031HP:0410031Submucous cleft of soft and hard palate0ZMPSTE24 CL E G H1026912877OMIM:275210Restrictive dermopathy, lethal83
HP:0410031HP:0000176Submucous cleft hard palate1AMER1 CL E G H13928526837ORPHA:2780Osteopathia striata-cranial sclerosis syndromeHP:0040282 - Frequent34
HP:0410031HP:0000176Submucous cleft hard palate1AMMECR1 CL E G H9949467OMIM:300990Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis2
HP:0410031HP:0000176Submucous cleft hard palate1B3GALNT2 CL E G H14878928596ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional43
HP:0410031HP:0000176Submucous cleft hard palate1B4GAT1 CL E G H1104115685ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional17
HP:0410031HP:0000176Submucous cleft hard palate1BCOR CL E G H5488020893OMIM:300166Microphthalmia, syndromic 2101
HP:0410031HP:0000176Submucous cleft hard palate1BCOR CL E G H5488020893ORPHA:2712Oculofaciocardiodental syndromeHP:0040282 - Frequent101
HP:0410031HP:0000176Submucous cleft hard palate1BICRA CL E G H299984332OMIM:619325COFFIN-SIRIS SYNDROME 12; CSS122
HP:0410031HP:0000176Submucous cleft hard palate1BRAF CL E G H6731097ORPHA:1340Cardiofaciocutaneous syndromeHP:0040283 - Occasional276
HP:0410031HP:0000176Submucous cleft hard palate1BRAF CL E G H6731097OMIM:115150Cardiofaciocutaneous syndrome 1.276
HP:0410031HP:0000176Submucous cleft hard palate1CARS1 CL E G H8331493OMIM:618891MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME; MDBH
HP:0410031HP:0000176Submucous cleft hard palate1CDC45 CL E G H83181739ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional9
HP:0410031HP:0000176Submucous cleft hard palate1CDC6 CL E G H9901744ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional31
HP:0410031HP:0000176Submucous cleft hard palate1CDC6 CL E G H9901744OMIM:613805Meier-Gorlin syndrome 531
HP:0410031HP:0000176Submucous cleft hard palate1CDH11 CL E G H10091750ORPHA:1299Branchioskeletogenital syndromeHP:0040281 - Very frequent2
HP:0410031HP:0000176Submucous cleft hard palate1CDT1 CL E G H8162024576ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional50
HP:0410031HP:0000176Submucous cleft hard palate1COL2A1 CL E G H12802200OMIM:108300Stickler syndrome, type I284
HP:0410031HP:0000176Submucous cleft hard palate1COL4A1 CL E G H12822202ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional193
HP:0410031HP:0000176Submucous cleft hard palate1CRPPA CL E G H72992037276ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional
HP:0410031HP:0000176Submucous cleft hard palate1CUL3 CL E G H84522553OMIM:619239NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES; NEDAUS92
HP:0410031HP:0000176Submucous cleft hard palate1DAG1 CL E G H16052666ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional108
HP:0410031HP:0000176Submucous cleft hard palate1DGCR2 CL E G H99932845OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0000176Submucous cleft hard palate1DGCR6 CL E G H82142846OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0000176Submucous cleft hard palate1DGCR8 CL E G H544872847OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0000176Submucous cleft hard palate1DHCR24 CL E G H17182859ORPHA:35107DesmosterolosisHP:0040281 - Very frequent72
HP:0410031HP:0000176Submucous cleft hard palate1ESS2 CL E G H822016817OMIM:192430Velocardiofacial syndrome
HP:0410031HP:0000176Submucous cleft hard palate1FKRP CL E G H7914717997ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional157
HP:0410031HP:0000176Submucous cleft hard palate1FKTN CL E G H22183622ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional184
HP:0410031HP:0000176Submucous cleft hard palate1FOXP2 CL E G H9398613875ORPHA:209908Childhood apraxia of speechHP:0040284 - Very rare143
HP:0410031HP:0000176Submucous cleft hard palate1GDF11 CL E G H102204216OMIM:619122VERTEBRAL HYPERSEGMENTATION AND OROFACIAL ANOMALIES; VHO
HP:0410031HP:0000176Submucous cleft hard palate1GMNN CL E G H5105317493ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional3
HP:0410031HP:0000176Submucous cleft hard palate1HAAO CL E G H234984796OMIM:617660Vertebral, cardiac, renal, and limb defects syndrome 12
HP:0410031HP:0000176Submucous cleft hard palate1HS2ST1 CL E G H96535193OMIM:619194NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS; NFSRA
HP:0410031HP:0000176Submucous cleft hard palate1HYAL1 CL E G H33735320OMIM:601492Mucopolysaccharidosis type IX28
HP:0410031HP:0000176Submucous cleft hard palate1HYLS1 CL E G H21984426558ORPHA:2189HydrolethalusHP:0040282 - Frequent31
HP:0410031HP:0000176Submucous cleft hard palate1KAT5 CL E G H105245275OMIM:619103NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB1
HP:0410031HP:0000176Submucous cleft hard palate1KAT6B CL E G H2352217582ORPHA:3047Blepharophimosis-intellectual disability syndrome, SBBYS typeHP:0040282 - Frequent141
HP:0410031HP:0000176Submucous cleft hard palate1KIF7 CL E G H37465430497ORPHA:2189HydrolethalusHP:0040282 - Frequent167
HP:0410031HP:0000176Submucous cleft hard palate1KRAS CL E G H38456407ORPHA:1340Cardiofaciocutaneous syndromeHP:0040283 - Occasional196
HP:0410031HP:0000176Submucous cleft hard palate1LARGE1 CL E G H92156511ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional136
HP:0410031HP:0000176Submucous cleft hard palate1LIG4 CL E G H39816601ORPHA:235Dubowitz syndromeHP:0040282 - Frequent88
HP:0410031HP:0000176Submucous cleft hard palate1LMNA CL E G H40006636ORPHA:1662Restrictive dermopathyHP:0040281 - Very frequent645
HP:0410031HP:0000176Submucous cleft hard palate1MAP2K1 CL E G H56046840ORPHA:1340Cardiofaciocutaneous syndromeHP:0040283 - Occasional134
HP:0410031HP:0000176Submucous cleft hard palate1MAP2K2 CL E G H56056842ORPHA:1340Cardiofaciocutaneous syndromeHP:0040283 - Occasional178
HP:0410031HP:0000176Submucous cleft hard palate1NSUN2 CL E G H5488825994ORPHA:235Dubowitz syndromeHP:0040282 - Frequent84
HP:0410031HP:0000176Submucous cleft hard palate1ORC1 CL E G H49988487ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional53
HP:0410031HP:0000176Submucous cleft hard palate1ORC4 CL E G H50008490ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional21
HP:0410031HP:0000176Submucous cleft hard palate1ORC6 CL E G H2359417151ORPHA:2554Ear-patella-short stature syndromeHP:0040283 - Occasional39
HP:0410031HP:0000176Submucous cleft hard palate1PIEZO2 CL E G H6389526270OMIM:114300Arthrogryposis, distal, type 3.77
HP:0410031HP:0000176Submucous cleft hard palate1PIEZO2 CL E G H6389526270ORPHA:2461Marden-Walker syndromeHP:0040281 - Very frequent77
HP:0410031HP:0000176Submucous cleft hard palate1POMGNT1 CL E G H5562419139ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional180
HP:0410031HP:0000176Submucous cleft hard palate1POMGNT2 CL E G H8489225902ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional33
HP:0410031HP:0000176Submucous cleft hard palate1POMK CL E G H8419726267ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional18
HP:0410031HP:0000176Submucous cleft hard palate1POMT1 CL E G H105859202ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional213
HP:0410031HP:0000176Submucous cleft hard palate1POMT2 CL E G H2995419743ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional221
HP:0410031HP:0000176Submucous cleft hard palate1PPP2R5D CL E G H55289312ORPHA:457279Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndromeHP:0040284 - Very rare10
HP:0410031HP:0000176Submucous cleft hard palate1PRKAR1B CL E G H55759390OMIM:619680MARBACH-SCHAAF NEURODEVELOPMENTAL SYNDROME; MASNS2
HP:0410031HP:0000176Submucous cleft hard palate1PRR12 CL E G H5747929217OMIM:619539NEUROOCULAR SYNDROME; NOC1
HP:0410031HP:0000176Submucous cleft hard palate1PTDSS1 CL E G H97919587ORPHA:2658Lenz-Majewski hyperostotic dwarfismHP:0040283 - Occasional6
HP:0410031HP:0000176Submucous cleft hard palate1RAD21 CL E G H58859811OMIM:614701Cornelia de Lange syndrome 425
HP:0410031HP:0000176Submucous cleft hard palate1RNU4ATAC CL E G H10015168334016ORPHA:2636Microcephalic osteodysplastic primordial dwarfism types I and IIIHP:0040282 - Frequent15
HP:0410031HP:0000176Submucous cleft hard palate1RPS23 CL E G H622810410OMIM:617412BRACHYCEPHALY, TRICHOMEGALY, AND DEVELOPMENTAL DELAY; BTDD2
HP:0410031HP:0000176Submucous cleft hard palate1RXYLT1 CL E G H1032913530ORPHA:899Walker-Warburg syndromeHP:0040283 - Occasional
HP:0410031HP:0000176Submucous cleft hard palate1SET CL E G H641810760OMIM:618106Mental retardation, autosomal dominant 581
HP:0410031HP:0000176Submucous cleft hard palate1SIAH1 CL E G H647710857OMIM:619314BURATTI-HAREL SYNDROME; BURHAS
HP:0410031HP:0000176Submucous cleft hard palate1SIX3 CL E G H649610889OMIM:157170Holoprosencephaly 2.32
HP:0410031HP:0000176Submucous cleft hard palate1SMAD4 CL E G H40896770ORPHA:2588Myhre syndromeHP:0040283 - Occasional504
HP:0410031HP:0000176Submucous cleft hard palate1SMCHD1 CL E G H2334729090ORPHA:2250Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndromeHP:0040283 - Occasional174
HP:0410031HP:0000176Submucous cleft hard palate1SON CL E G H665111183OMIM:617140Zttk syndrome12
HP:0410031HP:0000176Submucous cleft hard palate1SOX6 CL E G H5555316421OMIM:618971TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS1
HP:0410031HP:0000176Submucous cleft hard palate1SOX9 CL E G H666211204OMIM:114290Campomelic dysplasia109
HP:0410031HP:0000176Submucous cleft hard palate1STAG2 CL E G H1073511355OMIM:301043HOLOPROSENCEPHALY 13, X-LINKED; HPE131
HP:0410031HP:0000176Submucous cleft hard palate1TBX1 CL E G H689911592OMIM:192430Velocardiofacial syndrome32
HP:0410031HP:0000176Submucous cleft hard palate1TCTN3 CL E G H2612324519ORPHA:2753Orofaciodigital syndrome type 4HP:0040282 - Frequent31
HP:0410031HP:0000176Submucous cleft hard palate1WBP11 CL E G H5172916461OMIM:619227VERTEBRAL, CARDIAC, TRACHEOESOPHAGEAL, RENAL, AND LIMB DEFECTS; VCTERL
HP:0410031HP:0000176Submucous cleft hard palate1ZEB2 CL E G H983914881OMIM:235730Mowat-Wilson syndrome.362
HP:0410031HP:0000176Submucous cleft hard palate1ZMPSTE24 CL E G H1026912877ORPHA:1662Restrictive dermopathyHP:0040281 - Very frequent83
HP:0410031HP:0000176Submucous cleft hard palate1ZMPSTE24 CL E G H1026912877OMIM:275210Restrictive dermopathy, lethal.83


Genes (72) :AMER1 AMMECR1 B3GALNT2 B4GAT1 BCOR BICRA BRAF CARS1 CDC45 CDC6 CDH11 CDT1 COL2A1 COL4A1 CRPPA CUL3 DAG1 DGCR2 DGCR6 DGCR8 DHCR24 ESS2 FKRP FKTN FOXP2 GDF11 GMNN HAAO HS2ST1 HYAL1 HYLS1 KAT5 KAT6B KIF7 KRAS LARGE1 LIG4 LMNA MAP2K1 MAP2K2 NSUN2 ORC1 ORC4 ORC6 PIEZO2 POMGNT1 POMGNT2 POMK POMT1 POMT2 PPP2R5D PRKAR1B PRR12 PTDSS1 RAD21 RNU4ATAC RPS23 RXYLT1 SET SIAH1 SIX3 SMAD4 SMCHD1 SON SOX6 SOX9 STAG2 TBX1 TCTN3 WBP11 ZEB2 ZMPSTE24

Diseases (50) :ORPHA:2780 OMIM:300990 ORPHA:899 OMIM:300166 ORPHA:2712 OMIM:619325 ORPHA:1340 OMIM:115150 OMIM:618891 ORPHA:2554 OMIM:613805 ORPHA:1299 OMIM:108300 OMIM:619239 OMIM:192430 ORPHA:35107 ORPHA:209908 OMIM:619122 OMIM:617660 OMIM:619194 OMIM:601492 ORPHA:2189 OMIM:619103 ORPHA:3047 ORPHA:235 ORPHA:1662 OMIM:114300 ORPHA:2461 ORPHA:457279 OMIM:619680 OMIM:619539 ORPHA:2658 OMIM:614701 ORPHA:2636 OMIM:617412 OMIM:618106 OMIM:619314 OMIM:157170 ORPHA:2588 ORPHA:2250 OMIM:617140 OMIM:618971 OMIM:114290 OMIM:301043 ORPHA:2753 OMIM:619227 OMIM:235730 ORPHA:261552 ORPHA:261537 OMIM:275210
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.